Canonical Allele Identifier: CA1619116354

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353954_31353955delinsCA , CM000668.2:g.31353954_31353955delinsCA	GRCh38
NC_000006.11:g.31321731_31321732delinsCA , CM000668.1:g.31321731_31321732delinsCA	GRCh37
NC_000006.10:g.31429710_31429711delinsCA	NCBI36
NG_023187.1:g.8258_8259delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3482_3483delinsTG
ENST00000481849.6:n.3442_3443delinsTG
ENST00000497377.6:n.3349_3350delinsTG
ENST00000696558.1:c.1504_1505delinsTG	ENSP00000512716.1:n.1504_1505delinsTG
ENST00000696559.1:c.*346_*347delinsTG	ENSP00000512717.1:n.*346_*347delinsTG
ENST00000696560.1:c.*346_*347delinsTG	ENSP00000512718.1:n.*346_*347delinsTG
ENST00000696561.1:c.*346_*347delinsTG	ENSP00000512719.1:n.*346_*347delinsTG
ENST00000696562.1:c.*346_*347delinsTG	ENSP00000512720.1:n.*346_*347delinsTG
ENST00000412585.7:c.*346_*347delinsTG MANE Select	ENSP00000399168.2:n.*346_*347delinsTG
ENST00000412585.6:c.*346_*347delinsTG	ENSP00000399168.2:n.*346_*347delinsTG
ENST00000481849.5:n.670_671delinsTG
ENST00000497377.5:n.834_835delinsTG
NM_005514.6:c.*346_*347delinsTG	NP_005505.2:n.*346_*347delinsTG
XM_011514556.1:c.*346_*347delinsTG	XP_011512858.1:n.*346_*347delinsTG
XM_011514557.1:c.*346_*347delinsTG	XP_011512859.1:n.*346_*347delinsTG
XR_926175.1:n.1874_1875delinsTG
NM_005514.7:c.*346_*347delinsTG	NP_005505.2:n.*346_*347delinsTG
NM_005514.8:c.*346_*347delinsTG MANE Select	NP_005505.2:n.*346_*347delinsTG