Canonical Allele Identifier: CA014328

Linked Data

dbSNP Id: rs267608114

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47806356_47806357del , CM000664.2:g.47806356_47806357del GRCh38
NC_000002.11:g.48033495_48033496del , CM000664.1:g.48033495_48033496del GRCh37
NC_000002.10:g.47886999_47887000del NCBI36
NG_007111.1:g.28210_28211del , LRG_219:g.28210_28211del
NG_008397.1:g.104321_104322del

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.3502_3503del (MSH6) ENSP00000406248.2:p.Met1168GlyfsTer7
ENST00000420813.6:c.3502_3503del (MSH6) ENSP00000390382.2:p.Met1168GlyfsTer7
ENST00000455383.6:c.3502_3503del (MSH6) ENSP00000397484.2:p.Met1168GlyfsTer7
ENST00000700004.2:c.3415_3416del (MSH6) ENSP00000514752.2:p.Met1139GlyfsTer7
ENST00000699999.1:n.4473_4474del (MSH6)
ENST00000700000.1:c.2233_2234del (MSH6) ENSP00000514749.1:p.Met745GlyfsTer7
ENST00000700002.1:c.3805_3806del (MSH6) ENSP00000514750.1:p.Met1269GlyfsTer7
ENST00000700003.1:c.1254_1255del (MSH6) ENSP00000514751.1:n.1254_1255del
ENST00000700004.1:c.2572_2573del (MSH6) ENSP00000514752.1:p.Met858GlyfsTer7
ENST00000700005.1:n.2650_2651del (MSH6)
ENST00000700006.1:n.4957_4958del (MSH6)
ENST00000700007.1:n.2394_2395del (MSH6)
ENST00000700008.1:n.1968_1969del (MSH6)
ENST00000700009.1:n.2463_2464del (MSH6)
ENST00000700010.1:n.1208_1209del (MSH6)
ENST00000700011.1:n.3093_3094del (MSH6)
ENST00000682451.1:n.4393_4394del (FBXO11)
ENST00000684712.1:n.4655_4656del (FBXO11)
ENST00000234420.11:c.3799_3800del (MSH6) MANE Select ENSP00000234420.5:p.Met1267GlyfsTer7
ENST00000540021.6:c.3409_3410del (MSH6) ENSP00000446475.1:p.Met1137GlyfsTer7
ENST00000652107.1:c.3502_3503del (MSH6) ENSP00000498629.1:p.Met1168GlyfsTer7
ENST00000673637.1:c.3502_3503del (MSH6) ENSP00000501310.1:p.Met1168GlyfsTer7
ENST00000234420.9:c.3799_3800del (MSH6) ENSP00000234420.4:p.Met1267GlyfsTer7
ENST00000405808.5:c.169+1840_169+1841del (FBXO11) ENSP00000385127.1:n.169+1840_169+1841del
ENST00000434234.5:c.*124+1639_*124+1640del (FBXO11) ENSP00000402692.1:n.*124+1639_*124+1640de...
ENST00000445503.5:c.*3146_*3147del (MSH6) ENSP00000405294.1:n.*3146_*3147del
ENST00000538136.1:c.2893_2894del (MSH6) ENSP00000438580.1:p.Met965GlyfsTer7
ENST00000540021.5:c.3409_3410del (MSH6) ENSP00000446475.1:p.Met1137GlyfsTer7
ENST00000614496.4:c.2893_2894del (MSH6) ENSP00000477844.1:p.Met965GlyfsTer7
ENST00000622629.4:c.700_701del (MSH6) ENSP00000482078.1:p.Met234GlyfsTer7
NM_000179.2:c.3799_3800del , LRG_219t1:c.3799_3800del (MSH6) NP_000170.1:p.Met1267GlyfsTer7
NM_001281492.1:c.3409_3410del (MSH6) NP_001268421.1:p.Met1137GlyfsTer7
NM_001281493.1:c.2893_2894del (MSH6) NP_001268422.1:p.Met965GlyfsTer7
NM_001281494.1:c.2893_2894del (MSH6) NP_001268423.1:p.Met965GlyfsTer7
XM_005264271.1:c.3502_3503del (MSH6) XP_005264328.1:p.Met1168GlyfsTer7
XM_011532798.1:c.3616_3617del (MSH6) XP_011531100.1:p.Met1206GlyfsTer7
XM_011532799.1:c.3502_3503del (MSH6) XP_011531101.1:p.Met1168GlyfsTer7
XM_011532800.1:c.3502_3503del (MSH6) XP_011531102.1:p.Met1168GlyfsTer7
XM_024452819.1:c.3799_3800del (MSH6) XP_024308587.1:p.Met1267GlyfsTer14
XM_024452820.1:c.3616_3617del (MSH6) XP_024308588.1:p.Met1206GlyfsTer14
XM_024452821.1:c.3502_3503del (MSH6) XP_024308589.1:p.Met1168GlyfsTer14
XM_024452822.1:c.2893_2894del (MSH6) XP_024308590.1:p.Met965GlyfsTer14
NM_000179.3:c.3799_3800del (MSH6) MANE Select NP_000170.1:p.Met1267GlyfsTer7
NM_001281492.2:c.3409_3410del (MSH6) NP_001268421.1:p.Met1137GlyfsTer7
NM_001281493.2:c.2893_2894del (MSH6) NP_001268422.1:p.Met965GlyfsTer7
NM_001281494.2:c.2893_2894del (MSH6) NP_001268423.1:p.Met965GlyfsTer7