Canonical Allele Identifier: CA2677957788

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356887-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356890_31356891del , CM000668.2:g.31356890_31356891del	GRCh38
NC_000006.11:g.31324667_31324668del , CM000668.1:g.31324667_31324668del	GRCh37
NC_000006.10:g.31432646_31432647del	NCBI36
NG_023187.1:g.5324_5325del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1615_1616del
ENST00000481849.6:n.1615_1616del
ENST00000497377.6:n.1615_1616del
ENST00000640094.2:c.142_143del	ENSP00000491275.2:p.Val49GlyfsTer?
ENST00000696558.1:c.142_143del	ENSP00000512716.1:p.Val49GlyfsTer?
ENST00000696559.1:c.142_143del	ENSP00000512717.1:p.Val49GlyfsTer?
ENST00000696560.1:c.142_143del	ENSP00000512718.1:p.Val49GlyfsTer?
ENST00000696561.1:c.142_143del	ENSP00000512719.1:p.Val49GlyfsTer?
ENST00000696562.1:c.142_143del	ENSP00000512720.1:p.Val49GlyfsTer?
ENST00000412585.7:c.142_143del MANE Select	ENSP00000399168.2:p.Val49GlyfsTer?
ENST00000412585.6:c.142_143del	ENSP00000399168.2:p.Val49GlyfsTer?
ENST00000434333.1:c.175_176del	ENSP00000405931.1:p.Val60GlyfsTer?
ENST00000474381.1:n.17_18del
ENST00000498007.1:n.163_164del
ENST00000603274.1:n.244_245del
NM_005514.6:c.142_143del	NP_005505.2:p.Val49GlyfsTer?
XM_011514556.1:c.175_176del	XP_011512858.1:p.Val60GlyfsTer?
XM_011514557.1:c.142_143del	XP_011512859.1:p.Val49GlyfsTer?
XR_926175.1:n.152_153del
NM_005514.7:c.142_143del	NP_005505.2:p.Val49GlyfsTer?
NM_005514.8:c.142_143del MANE Select	NP_005505.2:p.Val49GlyfsTer?