Canonical Allele Identifier: CA2677957766

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356827-T-TCATC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356828_31356829insATCC , CM000668.2:g.31356828_31356829insATCC	GRCh38
NC_000006.11:g.31324605_31324606insATCC , CM000668.1:g.31324605_31324606insATCC	GRCh37
NC_000006.10:g.31432584_31432585insATCC	NCBI36
NG_023187.1:g.5385_5386insGATG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1676_1677insGATG
ENST00000481849.6:n.1676_1677insGATG
ENST00000497377.6:n.1676_1677insGATG
ENST00000640094.2:c.203_204insGATG	ENSP00000491275.2:p.Glu69MetfsTer31
ENST00000696558.1:c.203_204insGATG	ENSP00000512716.1:p.Glu69MetfsTer31
ENST00000696559.1:c.203_204insGATG	ENSP00000512717.1:p.Glu69MetfsTer31
ENST00000696560.1:c.203_204insGATG	ENSP00000512718.1:p.Glu69MetfsTer31
ENST00000696561.1:c.203_204insGATG	ENSP00000512719.1:p.Glu69MetfsTer31
ENST00000696562.1:c.203_204insGATG	ENSP00000512720.1:p.Glu69MetfsTer31
ENST00000412585.7:c.203_204insGATG MANE Select	ENSP00000399168.2:p.Glu69MetfsTer31
ENST00000412585.6:c.203_204insGATG	ENSP00000399168.2:p.Glu69MetfsTer31
ENST00000434333.1:c.236_237insGATG	ENSP00000405931.1:p.Glu80MetfsTer31
ENST00000474381.1:n.78_79insGATG
ENST00000498007.1:n.224_225insGATG
ENST00000603274.1:n.182_183insATCC
NM_005514.6:c.203_204insGATG	NP_005505.2:p.Glu69MetfsTer31
XM_011514556.1:c.236_237insGATG	XP_011512858.1:p.Glu80MetfsTer31
XM_011514557.1:c.203_204insGATG	XP_011512859.1:p.Glu69MetfsTer31
XR_926175.1:n.213_214insGATG
NM_005514.7:c.203_204insGATG	NP_005505.2:p.Glu69MetfsTer31
NM_005514.8:c.203_204insGATG MANE Select	NP_005505.2:p.Glu69MetfsTer31