Canonical Allele Identifier: CA1619112463

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356592_31356593delinsAG , CM000668.2:g.31356592_31356593delinsAG	GRCh38
NC_000006.11:g.31324369_31324370delinsAG , CM000668.1:g.31324369_31324370delinsAG	GRCh37
NC_000006.10:g.31432348_31432349delinsAG	NCBI36
NG_023187.1:g.5620_5621delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1816+95_1816+96delinsCT
ENST00000481849.6:n.1816+95_1816+96delinsCT
ENST00000497377.6:n.1816+95_1816+96delinsCT
ENST00000640094.2:c.343+95_343+96delinsCT	ENSP00000491275.2:n.343+95_343+96delinsCT
ENST00000696558.1:c.343+95_343+96delinsCT	ENSP00000512716.1:n.343+95_343+96delinsCT
ENST00000696559.1:c.343+95_343+96delinsCT	ENSP00000512717.1:n.343+95_343+96delinsCT
ENST00000696560.1:c.343+95_343+96delinsCT	ENSP00000512718.1:n.343+95_343+96delinsCT
ENST00000696561.1:c.343+95_343+96delinsCT	ENSP00000512719.1:n.343+95_343+96delinsCT
ENST00000696562.1:c.343+95_343+96delinsCT	ENSP00000512720.1:n.343+95_343+96delinsCT
ENST00000412585.7:c.343+95_343+96delinsCT MANE Select	ENSP00000399168.2:n.343+95_343+96delinsCT
ENST00000412585.6:c.343+95_343+96delinsCT	ENSP00000399168.2:n.343+95_343+96delinsCT
ENST00000434333.1:c.376+95_376+96delinsCT	ENSP00000405931.1:n.376+95_376+96delinsCT
ENST00000474381.1:n.218+95_218+96delinsCT
ENST00000498007.1:n.459_460delinsCT
NM_005514.6:c.343+95_343+96delinsCT	NP_005505.2:n.343+95_343+96delinsCT
XM_011514556.1:c.376+95_376+96delinsCT	XP_011512858.1:n.376+95_376+96delinsCT
XM_011514557.1:c.343+95_343+96delinsCT	XP_011512859.1:n.343+95_343+96delinsCT
XR_926175.1:n.353+95_353+96delinsCT
NM_005514.7:c.343+95_343+96delinsCT	NP_005505.2:n.343+95_343+96delinsCT
NM_005514.8:c.343+95_343+96delinsCT MANE Select	NP_005505.2:n.343+95_343+96delinsCT