Canonical Allele Identifier: CA2677957764

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356827-T-TCGGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356828_31356829insGGACC , CM000668.2:g.31356828_31356829insGGACC	GRCh38
NC_000006.11:g.31324605_31324606insGGACC , CM000668.1:g.31324605_31324606insGGACC	GRCh37
NC_000006.10:g.31432584_31432585insGGACC	NCBI36
NG_023187.1:g.5385_5386insGTCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1676_1677insGTCCG
ENST00000481849.6:n.1676_1677insGTCCG
ENST00000497377.6:n.1676_1677insGTCCG
ENST00000640094.2:c.203_204insGTCCG	ENSP00000491275.2:p.Glu69SerfsTer10
ENST00000696558.1:c.203_204insGTCCG	ENSP00000512716.1:p.Glu69SerfsTer10
ENST00000696559.1:c.203_204insGTCCG	ENSP00000512717.1:p.Glu69SerfsTer10
ENST00000696560.1:c.203_204insGTCCG	ENSP00000512718.1:p.Glu69SerfsTer10
ENST00000696561.1:c.203_204insGTCCG	ENSP00000512719.1:p.Glu69SerfsTer10
ENST00000696562.1:c.203_204insGTCCG	ENSP00000512720.1:p.Glu69SerfsTer10
ENST00000412585.7:c.203_204insGTCCG MANE Select	ENSP00000399168.2:p.Glu69SerfsTer10
ENST00000412585.6:c.203_204insGTCCG	ENSP00000399168.2:p.Glu69SerfsTer10
ENST00000434333.1:c.236_237insGTCCG	ENSP00000405931.1:p.Glu80SerfsTer10
ENST00000474381.1:n.78_79insGTCCG
ENST00000498007.1:n.224_225insGTCCG
ENST00000603274.1:n.182_183insGGACC
NM_005514.6:c.203_204insGTCCG	NP_005505.2:p.Glu69SerfsTer10
XM_011514556.1:c.236_237insGTCCG	XP_011512858.1:p.Glu80SerfsTer10
XM_011514557.1:c.203_204insGTCCG	XP_011512859.1:p.Glu69SerfsTer10
XR_926175.1:n.213_214insGTCCG
NM_005514.7:c.203_204insGTCCG	NP_005505.2:p.Glu69SerfsTer10
NM_005514.8:c.203_204insGTCCG MANE Select	NP_005505.2:p.Glu69SerfsTer10