Canonical Allele Identifier: CA2677957791

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356889-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356889_31356890insT , CM000668.2:g.31356889_31356890insT	GRCh38
NC_000006.11:g.31324666_31324667insT , CM000668.1:g.31324666_31324667insT	GRCh37
NC_000006.10:g.31432645_31432646insT	NCBI36
NG_023187.1:g.5323_5324insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1614_1615insA
ENST00000481849.6:n.1614_1615insA
ENST00000497377.6:n.1614_1615insA
ENST00000640094.2:c.141_142insA	ENSP00000491275.2:p.Ser48IlefsTer?
ENST00000696558.1:c.141_142insA	ENSP00000512716.1:p.Ser48IlefsTer?
ENST00000696559.1:c.141_142insA	ENSP00000512717.1:p.Ser48IlefsTer?
ENST00000696560.1:c.141_142insA	ENSP00000512718.1:p.Ser48IlefsTer?
ENST00000696561.1:c.141_142insA	ENSP00000512719.1:p.Ser48IlefsTer?
ENST00000696562.1:c.141_142insA	ENSP00000512720.1:p.Ser48IlefsTer?
ENST00000412585.7:c.141_142insA MANE Select	ENSP00000399168.2:p.Ser48IlefsTer?
ENST00000412585.6:c.141_142insA	ENSP00000399168.2:p.Ser48IlefsTer?
ENST00000434333.1:c.174_175insA	ENSP00000405931.1:p.Ser59IlefsTer?
ENST00000474381.1:n.16_17insA
ENST00000498007.1:n.162_163insA
ENST00000603274.1:n.243_244insT
NM_005514.6:c.141_142insA	NP_005505.2:p.Ser48IlefsTer?
XM_011514556.1:c.174_175insA	XP_011512858.1:p.Ser59IlefsTer?
XM_011514557.1:c.141_142insA	XP_011512859.1:p.Ser48IlefsTer?
XR_926175.1:n.151_152insA
NM_005514.7:c.141_142insA	NP_005505.2:p.Ser48IlefsTer?
NM_005514.8:c.141_142insA MANE Select	NP_005505.2:p.Ser48IlefsTer?