Canonical Allele Identifier: CA2677956613

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356259-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356261_31356262del , CM000668.2:g.31356261_31356262del	GRCh38
NC_000006.11:g.31324038_31324039del , CM000668.1:g.31324038_31324039del	GRCh37
NC_000006.10:g.31432017_31432018del	NCBI36
NG_023187.1:g.5952_5953del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1998_1999del
ENST00000481849.6:n.1998_1999del
ENST00000497377.6:n.1998_1999del
ENST00000640094.2:c.525_526del	ENSP00000491275.2:p.Glu176GlyfsTer?
ENST00000696558.1:c.525_526del	ENSP00000512716.1:p.Glu176GlyfsTer?
ENST00000696559.1:c.525_526del	ENSP00000512717.1:p.Glu176GlyfsTer?
ENST00000696560.1:c.525_526del	ENSP00000512718.1:p.Glu176GlyfsTer?
ENST00000696561.1:c.525_526del	ENSP00000512719.1:p.Glu176GlyfsTer?
ENST00000696562.1:c.525_526del	ENSP00000512720.1:p.Glu176GlyfsTer?
ENST00000412585.7:c.525_526del MANE Select	ENSP00000399168.2:p.Glu176GlyfsTer?
ENST00000412585.6:c.525_526del	ENSP00000399168.2:p.Glu176GlyfsTer?
ENST00000434333.1:c.558_559del	ENSP00000405931.1:p.Glu187GlyfsTer?
ENST00000474381.1:n.400_401del
ENST00000498007.1:n.791_792del
NM_005514.6:c.525_526del	NP_005505.2:p.Glu176GlyfsTer?
XM_011514556.1:c.558_559del	XP_011512858.1:p.Glu187GlyfsTer?
XM_011514557.1:c.525_526del	XP_011512859.1:p.Glu176GlyfsTer?
XR_926175.1:n.535_536del
NM_005514.7:c.525_526del	NP_005505.2:p.Glu176GlyfsTer?
NM_005514.8:c.525_526del MANE Select	NP_005505.2:p.Glu176GlyfsTer?