Canonical Allele Identifier: CA1172054000

Linked Data

dbSNP Id: rs112796068

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.64833237_64833238del , CM000663.2:g.64833237_64833238del GRCh38
NC_000001.10:g.65298920_65298921del , CM000663.1:g.65298920_65298921del GRCh37
NC_000001.9:g.65071508_65071509del NCBI36
NG_023402.1:g.138268_138269del
NG_023402.2:g.239510_239511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000465376.7:n.3130_3131del (JAK1)
ENST00000671746.2:c.*4698_*4699del (JAK1) ENSP00000500065.1:n.*4698_*4699del
ENST00000671929.2:c.*1325_*1326del (JAK1) ENSP00000500485.1:n.*1325_*1326del
ENST00000671954.2:c.*1325_*1326del (JAK1) ENSP00000500841.1:n.*1325_*1326del
ENST00000672179.2:c.*1325_*1326del (JAK1) ENSP00000500296.1:n.*1325_*1326del
ENST00000672247.2:c.*1325_*1326del (JAK1) ENSP00000499884.1:n.*1325_*1326del
ENST00000672434.2:c.*1325_*1326del (JAK1) ENSP00000499900.1:n.*1325_*1326del
ENST00000672574.2:c.*1325_*1326del (JAK1) ENSP00000500714.2:n.*1325_*1326del
ENST00000672751.2:c.*1325_*1326del (JAK1) ENSP00000500745.2:n.*1325_*1326del
ENST00000673246.2:c.*1325_*1326del (JAK1) ENSP00000499942.2:n.*1325_*1326del
ENST00000673314.2:n.6089_6090del (JAK1)
ENST00000673502.2:n.6249_6250del (JAK1)
ENST00000699259.1:c.*1325_*1326del (JAK1) ENSP00000514240.1:n.*1325_*1326del
ENST00000699260.1:c.*1325_*1326del (JAK1) ENSP00000514241.1:n.*1325_*1326del
ENST00000699261.1:c.*2164_*2165del (JAK1) ENSP00000514242.1:n.*2164_*2165del
ENST00000699310.1:c.*1325_*1326del (JAK1) ENSP00000514289.1:n.*1325_*1326del
ENST00000699311.1:c.*3450_*3451del (JAK1) ENSP00000514290.1:n.*3450_*3451del
ENST00000699312.1:c.*1325_*1326del (JAK1) ENSP00000514291.1:n.*1325_*1326del
ENST00000699313.1:c.*3299_*3300del (JAK1) ENSP00000514292.1:n.*3299_*3300del
ENST00000342505.5:c.*1325_*1326del (JAK1) MANE Select ENSP00000343204.4:n.*1325_*1326del
ENST00000342505.4:c.*1325_*1326del (JAK1) ENSP00000343204.4:n.*1325_*1326del
NM_002227.2:c.*1325_*1326del (JAK1) NP_002218.2:n.*1325_*1326del
XM_005270841.1:c.*1325_*1326del (JAK1) XP_005270898.1:n.*1325_*1326del
XM_006710624.1:c.*1325_*1326del (JAK1) XP_006710687.1:n.*1325_*1326del
XM_011541395.1:c.*1325_*1326del (JAK1) XP_011539697.1:n.*1325_*1326del
NM_001320923.1:c.*1325_*1326del (JAK1) NP_001307852.1:n.*1325_*1326del
NM_001321852.1:c.*1325_*1326del (JAK1) NP_001308781.1:n.*1325_*1326del
NM_001321853.1:c.*1325_*1326del (JAK1) NP_001308782.1:n.*1325_*1326del
NM_001321854.1:c.*1325_*1326del (JAK1) NP_001308783.1:n.*1325_*1326del
NM_001321855.1:c.*1325_*1326del (JAK1) NP_001308784.1:n.*1325_*1326del
NM_001321856.1:c.*1325_*1326del (JAK1) NP_001308785.1:n.*1325_*1326del
NM_001321857.1:c.*1325_*1326del (JAK1) NP_001308786.1:n.*1325_*1326del
NM_002227.3:c.*1325_*1326del (JAK1) NP_002218.2:n.*1325_*1326del
XR_946693.3:n.4671_4672del (RAVER2)
NM_002227.4:c.*1325_*1326del (JAK1) MANE Select NP_002218.2:n.*1325_*1326del
NM_001321852.2:c.*1325_*1326del (JAK1) NP_001308781.1:n.*1325_*1326del
NM_001321853.2:c.*1325_*1326del (JAK1) NP_001308782.1:n.*1325_*1326del
NM_001321854.2:c.*1325_*1326del (JAK1) NP_001308783.1:n.*1325_*1326del
NM_001321855.2:c.*1325_*1326del (JAK1) NP_001308784.1:n.*1325_*1326del
NM_001321857.2:c.*1325_*1326del (JAK1) NP_001308786.1:n.*1325_*1326del
NM_001320923.2:c.*1325_*1326del (JAK1) NP_001307852.1:n.*1325_*1326del
NM_001321856.2:c.*1325_*1326del (JAK1) NP_001308785.1:n.*1325_*1326del