Canonical Allele Identifier: CA645561020
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356277_31356278insG , CM000668.2:g.31356277_31356278insG GRCh38
NC_000006.11:g.31324054_31324055insG , CM000668.1:g.31324054_31324055insG GRCh37
NC_000006.10:g.31432033_31432034insG NCBI36
NG_023187.1:g.5935_5936insC

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1981_1982insC
ENST00000481849.6:n.1981_1982insC
ENST00000497377.6:n.1981_1982insC
ENST00000640094.2:c.508_509insC ENSP00000491275.2:p.Lys170ThrfsTer7
ENST00000696558.1:c.508_509insC ENSP00000512716.1:p.Lys170ThrfsTer7
ENST00000696559.1:c.508_509insC ENSP00000512717.1:p.Lys170ThrfsTer7
ENST00000696560.1:c.508_509insC ENSP00000512718.1:p.Lys170ThrfsTer7
ENST00000696561.1:c.508_509insC ENSP00000512719.1:p.Lys170ThrfsTer7
ENST00000696562.1:c.508_509insC ENSP00000512720.1:p.Lys170ThrfsTer7
ENST00000412585.7:c.508_509insC MANE Select ENSP00000399168.2:p.Lys170ThrfsTer7
ENST00000412585.6:c.508_509insC ENSP00000399168.2:p.Lys170ThrfsTer7
ENST00000434333.1:c.541_542insC ENSP00000405931.1:p.Lys181ThrfsTer7
ENST00000474381.1:n.383_384insC
ENST00000498007.1:n.774_775insC
NM_005514.6:c.508_509insC NP_005505.2:p.Lys170ThrfsTer7
XM_011514556.1:c.541_542insC XP_011512858.1:p.Lys181ThrfsTer7
XM_011514557.1:c.508_509insC XP_011512859.1:p.Lys170ThrfsTer7
XR_926175.1:n.518_519insC
NM_005514.7:c.508_509insC NP_005505.2:p.Lys170ThrfsTer7
NM_005514.8:c.508_509insC MANE Select NP_005505.2:p.Lys170ThrfsTer7