Canonical Allele Identifier: CA1619117870

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354925_31354927delinsCCA , CM000668.2:g.31354925_31354927delinsCCA	GRCh38
NC_000006.11:g.31322702_31322704delinsCCA , CM000668.1:g.31322702_31322704delinsCCA	GRCh37
NC_000006.10:g.31430681_31430683delinsCCA	NCBI36
NG_023187.1:g.7286_7288delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+180_3059+182delinsTGG
ENST00000481849.6:n.2758_2760delinsTGG
ENST00000497377.6:n.2665_2667delinsTGG
ENST00000640094.2:c.896-262_896-260delinsTGG	ENSP00000491275.2:n.896-262_896-260delinsTGG
ENST00000696558.1:c.1081+180_1081+182delinsTGG	ENSP00000512716.1:n.1081+180_1081+182delinsTGG
ENST00000696559.1:c.1012+180_1012+182delinsTGG	ENSP00000512717.1:n.1012+180_1012+182delinsTGG
ENST00000696560.1:c.1012+180_1012+182delinsTGG	ENSP00000512718.1:n.1012+180_1012+182delinsTGG
ENST00000696561.1:c.1012+180_1012+182delinsTGG	ENSP00000512719.1:n.1012+180_1012+182delinsTGG
ENST00000696562.1:c.1012+180_1012+182delinsTGG	ENSP00000512720.1:n.1012+180_1012+182delinsTGG
ENST00000412585.7:c.1012+180_1012+182delinsTGG MANE Select	ENSP00000399168.2:n.1012+180_1012+182delinsTGG
ENST00000640094.1:c.89-262_89-260delinsTGG	ENSP00000491275.1:n.89-262_89-260delinsTGG
ENST00000412585.6:c.1012+180_1012+182delinsTGG	ENSP00000399168.2:n.1012+180_1012+182delinsTGG
ENST00000497377.5:n.150_152delinsTGG
NM_005514.6:c.1012+180_1012+182delinsTGG	NP_005505.2:n.1012+180_1012+182delinsTGG
XM_011514556.1:c.1045+180_1045+182delinsTGG	XP_011512858.1:n.1045+180_1045+182delinsTGG
XM_011514557.1:c.896-262_896-260delinsTGG	XP_011512859.1:n.896-262_896-260delinsTGG
XR_926175.1:n.1451+180_1451+182delinsTGG
NM_005514.7:c.1012+180_1012+182delinsTGG	NP_005505.2:n.1012+180_1012+182delinsTGG
NM_005514.8:c.1012+180_1012+182delinsTGG MANE Select	NP_005505.2:n.1012+180_1012+182delinsTGG