Canonical Allele Identifier: CA1087467547
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356245_31356246insAT , CM000668.2:g.31356245_31356246insAT GRCh38
NC_000006.11:g.31324022_31324023insAT , CM000668.1:g.31324022_31324023insAT GRCh37
NC_000006.10:g.31432001_31432002insAT NCBI36
NG_023187.1:g.5968_5969insTA

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2014_2015insTA
ENST00000481849.6:n.2014_2015insTA
ENST00000497377.6:n.2014_2015insTA
ENST00000640094.2:c.541_542insTA ENSP00000491275.2:p.Arg181IlefsTer?
ENST00000696558.1:c.541_542insTA ENSP00000512716.1:p.Arg181IlefsTer?
ENST00000696559.1:c.541_542insTA ENSP00000512717.1:p.Arg181IlefsTer?
ENST00000696560.1:c.541_542insTA ENSP00000512718.1:p.Arg181IlefsTer?
ENST00000696561.1:c.541_542insTA ENSP00000512719.1:p.Arg181IlefsTer?
ENST00000696562.1:c.541_542insTA ENSP00000512720.1:p.Arg181IlefsTer?
ENST00000412585.7:c.541_542insTA MANE Select ENSP00000399168.2:p.Arg181IlefsTer?
ENST00000412585.6:c.541_542insTA ENSP00000399168.2:p.Arg181IlefsTer?
ENST00000434333.1:c.574_575insTA ENSP00000405931.1:p.Arg192IlefsTer?
ENST00000474381.1:n.416_417insTA
ENST00000498007.1:n.807_808insTA
NM_005514.6:c.541_542insTA NP_005505.2:p.Arg181IlefsTer?
XM_011514556.1:c.574_575insTA XP_011512858.1:p.Arg192IlefsTer?
XM_011514557.1:c.541_542insTA XP_011512859.1:p.Arg181IlefsTer?
XR_926175.1:n.551_552insTA
NM_005514.7:c.541_542insTA NP_005505.2:p.Arg181IlefsTer?
NM_005514.8:c.541_542insTA MANE Select NP_005505.2:p.Arg181IlefsTer?