Canonical Allele Identifier: CA1619113071

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356764_31356767delinsCTGT , CM000668.2:g.31356764_31356767delinsCTGT	GRCh38
NC_000006.11:g.31324541_31324544delinsCTGT , CM000668.1:g.31324541_31324544delinsCTGT	GRCh37
NC_000006.10:g.31432520_31432523delinsCTGT	NCBI36
NG_023187.1:g.5446_5449delinsACAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1737_1740delinsACAG
ENST00000481849.6:n.1737_1740delinsACAG
ENST00000497377.6:n.1737_1740delinsACAG
ENST00000640094.2:c.264_267delinsACAG	ENSP00000491275.2:p.Thr88=
ENST00000696558.1:c.264_267delinsACAG	ENSP00000512716.1:p.Thr88=
ENST00000696559.1:c.264_267delinsACAG	ENSP00000512717.1:p.Thr88=
ENST00000696560.1:c.264_267delinsACAG	ENSP00000512718.1:p.Thr88=
ENST00000696561.1:c.264_267delinsACAG	ENSP00000512719.1:p.Thr88=
ENST00000696562.1:c.264_267delinsACAG	ENSP00000512720.1:p.Thr88=
ENST00000412585.7:c.264_267delinsACAG MANE Select	ENSP00000399168.2:p.Thr88=
ENST00000412585.6:c.264_267delinsACAG	ENSP00000399168.2:p.Thr88=
ENST00000434333.1:c.297_300delinsACAG	ENSP00000405931.1:p.Thr99=
ENST00000474381.1:n.139_142delinsACAG
ENST00000498007.1:n.285_288delinsACAG
ENST00000603274.1:n.118_121delinsCTGT
NM_005514.6:c.264_267delinsACAG	NP_005505.2:p.Thr88=
XM_011514556.1:c.297_300delinsACAG	XP_011512858.1:p.Thr99=
XM_011514557.1:c.264_267delinsACAG	XP_011512859.1:p.Thr88=
XR_926175.1:n.274_277delinsACAG
NM_005514.7:c.264_267delinsACAG	NP_005505.2:p.Thr88=
NM_005514.8:c.264_267delinsACAG MANE Select	NP_005505.2:p.Thr88=