Canonical Allele Identifier: CA2770503825

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356482_31356483insA , CM000668.2:g.31356482_31356483insA	GRCh38
NC_000006.11:g.31324259_31324260insA , CM000668.1:g.31324259_31324260insA	GRCh37
NC_000006.10:g.31432238_31432239insA	NCBI36
NG_023187.1:g.5730_5731insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1817-41_1817-40insT
ENST00000481849.6:n.1817-41_1817-40insT
ENST00000497377.6:n.1817-41_1817-40insT
ENST00000640094.2:c.344-41_344-40insT	ENSP00000491275.2:n.344-41_344-40insT
ENST00000696558.1:c.344-41_344-40insT	ENSP00000512716.1:n.344-41_344-40insT
ENST00000696559.1:c.344-41_344-40insT	ENSP00000512717.1:n.344-41_344-40insT
ENST00000696560.1:c.344-41_344-40insT	ENSP00000512718.1:n.344-41_344-40insT
ENST00000696561.1:c.344-41_344-40insT	ENSP00000512719.1:n.344-41_344-40insT
ENST00000696562.1:c.344-41_344-40insT	ENSP00000512720.1:n.344-41_344-40insT
ENST00000412585.7:c.344-41_344-40insT MANE Select	ENSP00000399168.2:n.344-41_344-40insT
ENST00000412585.6:c.344-41_344-40insT	ENSP00000399168.2:n.344-41_344-40insT
ENST00000434333.1:c.377-41_377-40insT	ENSP00000405931.1:n.377-41_377-40insT
ENST00000474381.1:n.219-41_219-40insT
ENST00000498007.1:n.569_570insT
NM_005514.6:c.344-41_344-40insT	NP_005505.2:n.344-41_344-40insT
XM_011514556.1:c.377-41_377-40insT	XP_011512858.1:n.377-41_377-40insT
XM_011514557.1:c.344-41_344-40insT	XP_011512859.1:n.344-41_344-40insT
XR_926175.1:n.354-41_354-40insT
NM_005514.7:c.344-41_344-40insT	NP_005505.2:n.344-41_344-40insT
NM_005514.8:c.344-41_344-40insT MANE Select	NP_005505.2:n.344-41_344-40insT