Canonical Allele Identifier: CA1298151032
Community Standard Title: NM_001164508.2(NEB):c.24401dup (p.Tyr8134Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.151496361dup , CM000664.2:g.151496361dup GRCh38
NC_000002.11:g.152352875dup , CM000664.1:g.152352875dup GRCh37
NC_000002.10:g.152061121dup NCBI36
NG_009382.2:g.243127dup , LRG_202:g.243127dup

Transcript Alleles

HGVS Amino-acid Change
NM_001164508.2:c.24401dup (NEB) MANE Select NP_001157980.2:p.Tyr8134Ter
ENST00000397345.8:c.24401dup (NEB) MANE Select ENSP00000380505.3:p.Tyr8134Ter
NM_001164507.2:c.24401dup (NEB) MANE Plus Clinical NP_001157979.2:p.Tyr8134Ter
ENST00000427231.7:c.24401dup (NEB) MANE Plus Clinical ENSP00000416578.2:p.Tyr8134Ter
NM_001164507.1:c.24401dup (NEB) NP_001157979.1:p.Tyr8134Ter
NM_001164508.1:c.24401dup (NEB) NP_001157980.1:p.Tyr8134Ter
NM_001271208.1:c.24506dup , LRG_202t1:c.24506dup (NEB) NP_001258137.1:p.Tyr8169Ter
NM_001271208.2:c.24506dup (NEB) NP_001258137.2:p.Tyr8169Ter
NM_004543.4:c.18833dup (NEB) NP_004534.2:p.Tyr6278Ter
NM_004543.5:c.18833dup (NEB) NP_004534.3:p.Tyr6278Ter
ENST00000172853.14:c.18833dup (NEB) ENSP00000172853.10:p.Tyr6278Ter
ENST00000397337.6:c.802dup (NEB)
ENST00000397345.7:c.24401dup (NEB) ENSP00000380505.3:p.Tyr8134Ter
ENST00000409198.5:c.18833dup (NEB) ENSP00000386259.1:p.Tyr6278Ter
ENST00000413693.5:c.8033dup (NEB) ENSP00000410961.1:p.Tyr2678Ter
ENST00000421461.6:c.837dup (NEB)
ENST00000424585.1:c.710dup (NEB) ENSP00000404876.1:p.Tyr237Ter
ENST00000427231.6:c.24401dup (NEB) ENSP00000416578.2:p.Tyr8134Ter
ENST00000434685.5:c.1395-2108dup (NEB)
ENST00000434685.6:c.3075-3867dup (NEB)
ENST00000454583.6:c.2753+1035dup (RIF1)
ENST00000457745.1:n.578+1035dup (RIF1)
ENST00000484077.1:n.352+1035dup (RIF1)
ENST00000498015.2:n.226-3867dup (NEB)
ENST00000603639.5:c.24401dup (NEB) ENSP00000473894.1:p.Tyr8134Ter
ENST00000604864.5:c.24401dup (NEB) ENSP00000474498.1:p.Tyr8134Ter
ENST00000618972.4:c.24506dup (NEB) ENSP00000484342.1:p.Tyr8169Ter
ENST00000688578.1:c.1000dup (NEB)
ENST00000690043.1:c.6378-2108dup (NEB)
ENST00000693000.1:n.2657-3867dup (NEB)
XM_005246590.1:c.24308dup (NEB) XP_005246647.1:p.Tyr8103Ter
XM_005246590.2:c.24308dup (NEB) XP_005246647.1:p.Tyr8103Ter
XM_005246591.1:c.24308dup (NEB) XP_005246648.1:p.Tyr8103Ter
XM_005246591.2:c.24308dup (NEB) XP_005246648.1:p.Tyr8103Ter
XM_005246592.1:c.24308dup (NEB) XP_005246649.1:p.Tyr8103Ter
XM_005246592.2:c.24308dup (NEB) XP_005246649.1:p.Tyr8103Ter
XM_005246593.1:c.24401dup (NEB) XP_005246650.1:p.Tyr8134Ter
XM_005246593.2:c.24401dup (NEB) XP_005246650.1:p.Tyr8134Ter
XM_005246594.1:c.24308dup (NEB) XP_005246651.1:p.Tyr8103Ter
XM_005246594.2:c.24308dup (NEB) XP_005246651.1:p.Tyr8103Ter
XM_005246595.1:c.24308dup (NEB) XP_005246652.1:p.Tyr8103Ter
XM_005246596.1:c.24215dup (NEB) XP_005246653.1:p.Tyr8072Ter
XM_005246596.2:c.24215dup (NEB) XP_005246653.1:p.Tyr8072Ter
XM_005246597.1:c.24300+1265dup (NEB) XP_005246654.1:n.24300+1265dup
XM_005246597.2:c.24300+1265dup (NEB) XP_005246654.1:n.24300+1265dup
XM_005246598.1:c.24401dup (NEB) XP_005246655.1:p.Tyr8134Ter
XM_005246598.2:c.24401dup (NEB) XP_005246655.1:p.Tyr8134Ter
XM_005246599.1:c.24122dup (NEB) XP_005246656.1:p.Tyr8041Ter
XM_005246599.2:c.24122dup (NEB) XP_005246656.1:p.Tyr8041Ter
XM_005246600.1:c.24122dup (NEB) XP_005246657.1:p.Tyr8041Ter
XM_005246601.1:c.24029dup (NEB) XP_005246658.1:p.Tyr8010Ter
XM_005246601.2:c.24029dup (NEB) XP_005246658.1:p.Tyr8010Ter
XM_005246602.1:c.24029dup (NEB) XP_005246659.1:p.Tyr8010Ter
XM_005246602.2:c.24029dup (NEB) XP_005246659.1:p.Tyr8010Ter
XM_005246603.1:c.23936dup (NEB) XP_005246660.1:p.Tyr7979Ter
XM_005246603.2:c.23936dup (NEB) XP_005246660.1:p.Tyr7979Ter
XM_005246604.1:c.24029dup (NEB) XP_005246661.1:p.Tyr8010Ter
XM_005246604.2:c.24029dup (NEB) XP_005246661.1:p.Tyr8010Ter
XM_005246606.1:c.23936dup (NEB) XP_005246663.1:p.Tyr7979Ter
XM_005246606.2:c.23936dup (NEB) XP_005246663.1:p.Tyr7979Ter
XM_005246608.1:c.23929-2108dup (NEB) XP_005246665.1:n.23929-2108dup
XM_005246608.2:c.23929-2108dup (NEB) XP_005246665.1:n.23929-2108dup
XM_005246610.1:c.23836-2108dup (NEB) XP_005246667.1:n.23836-2108dup
XM_005246610.2:c.23836-2108dup (NEB) XP_005246667.1:n.23836-2108dup
XM_005246611.1:c.24022-2916dup (NEB) XP_005246668.1:n.24022-2916dup
XM_005246611.2:c.24022-2916dup (NEB) XP_005246668.1:n.24022-2916dup
XM_005246612.1:c.23672dup (NEB) XP_005246669.1:p.Tyr7891Ter
XM_005246612.2:c.23672dup (NEB) XP_005246669.1:p.Tyr7891Ter
XM_005246613.1:c.23672dup (NEB) XP_005246670.1:p.Tyr7891Ter
XM_005246613.2:c.23672dup (NEB) XP_005246670.1:p.Tyr7891Ter
XM_005246615.1:c.23928+1265dup (NEB) XP_005246672.1:n.23928+1265dup
XM_005246615.2:c.23928+1265dup (NEB) XP_005246672.1:n.23928+1265dup
XM_005246617.1:c.21485dup (NEB) XP_005246674.1:p.Tyr7162Ter
XM_005246617.2:c.21485dup (NEB) XP_005246674.1:p.Tyr7162Ter
XM_006712541.1:c.23936dup (NEB) XP_006712604.1:p.Tyr7979Ter
XM_006712541.2:c.23936dup (NEB) XP_006712604.1:p.Tyr7979Ter
XM_006712542.1:c.24021+1265dup (NEB) XP_006712605.1:n.24021+1265dup
XM_006712542.2:c.24021+1265dup (NEB) XP_006712605.1:n.24021+1265dup
XM_011511224.1:c.24308dup (NEB) XP_011509526.1:p.Tyr8103Ter
XM_011511225.1:c.23743-2108dup (NEB) XP_011509527.1:n.23743-2108dup
XM_011511225.2:c.23743-2108dup (NEB) XP_011509527.1:n.23743-2108dup
XM_011511226.1:c.22214dup (NEB) XP_011509528.1:p.Tyr7405Ter
XM_011511226.2:c.22214dup (NEB) XP_011509528.1:p.Tyr7405Ter
XM_011511227.1:c.20027dup (NEB) XP_011509529.1:p.Tyr6676Ter
XM_011511227.2:c.20027dup (NEB) XP_011509529.1:p.Tyr6676Ter
XM_017004177.1:c.24290dup (NEB) XP_016859666.1:p.Tyr8097Ter
XM_017004178.1:c.24215dup (NEB) XP_016859667.1:p.Tyr8072Ter
XM_017004179.1:c.23936dup (NEB) XP_016859668.1:p.Tyr7979Ter
XM_017004180.1:c.23936dup (NEB) XP_016859669.1:p.Tyr7979Ter
XM_017004181.1:c.23843dup (NEB) XP_016859670.1:p.Tyr7948Ter
XM_017004182.1:c.23843dup (NEB) XP_016859671.1:p.Tyr7948Ter
XM_017004183.1:c.23836-2108dup (NEB) XP_016859672.1:n.23836-2108dup
XM_017004184.1:c.23843dup (NEB) XP_016859673.1:p.Tyr7948Ter
XM_017004185.1:c.23743-3867dup (NEB) XP_016859674.1:n.23743-3867dup
XR_001738811.2:n.8311+1035dup (RIF1)
XR_001738812.2:n.8311+1035dup (RIF1)
XR_001738813.2:n.8214-1425dup (RIF1)
XR_001738814.2:n.8214-3044dup (RIF1)
XR_001738815.2:n.8214-6673dup (RIF1)
XR_001738816.2:n.8214-9849dup (RIF1)
XR_001738817.2:n.8213+13026dup (RIF1)
XR_922955.1:n.7838+13026dup (RIF1)
XR_922956.1:n.7936+1035dup (RIF1)
XR_922957.1:n.7839-1425dup (RIF1)