Canonical Allele Identifier: CA2677957609

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356710-G-GCGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356711_31356712insGGAC , CM000668.2:g.31356711_31356712insGGAC	GRCh38
NC_000006.11:g.31324488_31324489insGGAC , CM000668.1:g.31324488_31324489insGGAC	GRCh37
NC_000006.10:g.31432467_31432468insGGAC	NCBI36
NG_023187.1:g.5502_5503insTCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1793_1794insTCCG
ENST00000481849.6:n.1793_1794insTCCG
ENST00000497377.6:n.1793_1794insTCCG
ENST00000640094.2:c.320_321insTCCG	ENSP00000491275.2:p.Tyr108ProfsTer?
ENST00000696558.1:c.320_321insTCCG	ENSP00000512716.1:p.Tyr108ProfsTer?
ENST00000696559.1:c.320_321insTCCG	ENSP00000512717.1:p.Tyr108ProfsTer?
ENST00000696560.1:c.320_321insTCCG	ENSP00000512718.1:p.Tyr108ProfsTer?
ENST00000696561.1:c.320_321insTCCG	ENSP00000512719.1:p.Tyr108ProfsTer?
ENST00000696562.1:c.320_321insTCCG	ENSP00000512720.1:p.Tyr108ProfsTer?
ENST00000412585.7:c.320_321insTCCG MANE Select	ENSP00000399168.2:p.Tyr108ProfsTer?
ENST00000412585.6:c.320_321insTCCG	ENSP00000399168.2:p.Tyr108ProfsTer?
ENST00000434333.1:c.353_354insTCCG	ENSP00000405931.1:p.Tyr119ProfsTer?
ENST00000474381.1:n.195_196insTCCG
ENST00000498007.1:n.341_342insTCCG
ENST00000603274.1:n.65_66insGGAC
NM_005514.6:c.320_321insTCCG	NP_005505.2:p.Tyr108ProfsTer?
XM_011514556.1:c.353_354insTCCG	XP_011512858.1:p.Tyr119ProfsTer?
XM_011514557.1:c.320_321insTCCG	XP_011512859.1:p.Tyr108ProfsTer?
XR_926175.1:n.330_331insTCCG
NM_005514.7:c.320_321insTCCG	NP_005505.2:p.Tyr108ProfsTer?
NM_005514.8:c.320_321insTCCG MANE Select	NP_005505.2:p.Tyr108ProfsTer?