Canonical Allele Identifier: CA2677957763

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356827-T-TCGTC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356828_31356829insGTCC , CM000668.2:g.31356828_31356829insGTCC	GRCh38
NC_000006.11:g.31324605_31324606insGTCC , CM000668.1:g.31324605_31324606insGTCC	GRCh37
NC_000006.10:g.31432584_31432585insGTCC	NCBI36
NG_023187.1:g.5385_5386insGACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1676_1677insGACG
ENST00000481849.6:n.1676_1677insGACG
ENST00000497377.6:n.1676_1677insGACG
ENST00000640094.2:c.203_204insGACG	ENSP00000491275.2:p.Glu69ThrfsTer31
ENST00000696558.1:c.203_204insGACG	ENSP00000512716.1:p.Glu69ThrfsTer31
ENST00000696559.1:c.203_204insGACG	ENSP00000512717.1:p.Glu69ThrfsTer31
ENST00000696560.1:c.203_204insGACG	ENSP00000512718.1:p.Glu69ThrfsTer31
ENST00000696561.1:c.203_204insGACG	ENSP00000512719.1:p.Glu69ThrfsTer31
ENST00000696562.1:c.203_204insGACG	ENSP00000512720.1:p.Glu69ThrfsTer31
ENST00000412585.7:c.203_204insGACG MANE Select	ENSP00000399168.2:p.Glu69ThrfsTer31
ENST00000412585.6:c.203_204insGACG	ENSP00000399168.2:p.Glu69ThrfsTer31
ENST00000434333.1:c.236_237insGACG	ENSP00000405931.1:p.Glu80ThrfsTer31
ENST00000474381.1:n.78_79insGACG
ENST00000498007.1:n.224_225insGACG
ENST00000603274.1:n.182_183insGTCC
NM_005514.6:c.203_204insGACG	NP_005505.2:p.Glu69ThrfsTer31
XM_011514556.1:c.236_237insGACG	XP_011512858.1:p.Glu80ThrfsTer31
XM_011514557.1:c.203_204insGACG	XP_011512859.1:p.Glu69ThrfsTer31
XR_926175.1:n.213_214insGACG
NM_005514.7:c.203_204insGACG	NP_005505.2:p.Glu69ThrfsTer31
NM_005514.8:c.203_204insGACG MANE Select	NP_005505.2:p.Glu69ThrfsTer31