Canonical Allele Identifier: CA2677957717

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356760-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356760_31356761insT , CM000668.2:g.31356760_31356761insT	GRCh38
NC_000006.11:g.31324537_31324538insT , CM000668.1:g.31324537_31324538insT	GRCh37
NC_000006.10:g.31432516_31432517insT	NCBI36
NG_023187.1:g.5452_5453insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1743_1744insA
ENST00000481849.6:n.1743_1744insA
ENST00000497377.6:n.1743_1744insA
ENST00000640094.2:c.270_271insA	ENSP00000491275.2:p.Tyr91IlefsTer8
ENST00000696558.1:c.270_271insA	ENSP00000512716.1:p.Tyr91IlefsTer8
ENST00000696559.1:c.270_271insA	ENSP00000512717.1:p.Tyr91IlefsTer8
ENST00000696560.1:c.270_271insA	ENSP00000512718.1:p.Tyr91IlefsTer8
ENST00000696561.1:c.270_271insA	ENSP00000512719.1:p.Tyr91IlefsTer8
ENST00000696562.1:c.270_271insA	ENSP00000512720.1:p.Tyr91IlefsTer8
ENST00000412585.7:c.270_271insA MANE Select	ENSP00000399168.2:p.Tyr91IlefsTer8
ENST00000412585.6:c.270_271insA	ENSP00000399168.2:p.Tyr91IlefsTer8
ENST00000434333.1:c.303_304insA	ENSP00000405931.1:p.Tyr102IlefsTer8
ENST00000474381.1:n.145_146insA
ENST00000498007.1:n.291_292insA
ENST00000603274.1:n.114_115insT
NM_005514.6:c.270_271insA	NP_005505.2:p.Tyr91IlefsTer8
XM_011514556.1:c.303_304insA	XP_011512858.1:p.Tyr102IlefsTer8
XM_011514557.1:c.270_271insA	XP_011512859.1:p.Tyr91IlefsTer8
XR_926175.1:n.280_281insA
NM_005514.7:c.270_271insA	NP_005505.2:p.Tyr91IlefsTer8
NM_005514.8:c.270_271insA MANE Select	NP_005505.2:p.Tyr91IlefsTer8