Canonical Allele Identifier: CA2770503552

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354927_31354928insGGGCG , CM000668.2:g.31354927_31354928insGGGCG	GRCh38
NC_000006.11:g.31322704_31322705insGGGCG , CM000668.1:g.31322704_31322705insGGGCG	GRCh37
NC_000006.10:g.31430683_31430684insGGGCG	NCBI36
NG_023187.1:g.7285_7286insCGCCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+179_3059+180insCGCCC
ENST00000481849.6:n.2757_2758insCGCCC
ENST00000497377.6:n.2664_2665insCGCCC
ENST00000640094.2:c.896-263_896-262insCGCCC	ENSP00000491275.2:n.896-263_896-262insCGCCC
ENST00000696558.1:c.1081+179_1081+180insCGCCC	ENSP00000512716.1:n.1081+179_1081+180insCGCCC
ENST00000696559.1:c.1012+179_1012+180insCGCCC	ENSP00000512717.1:n.1012+179_1012+180insCGCCC
ENST00000696560.1:c.1012+179_1012+180insCGCCC	ENSP00000512718.1:n.1012+179_1012+180insCGCCC
ENST00000696561.1:c.1012+179_1012+180insCGCCC	ENSP00000512719.1:n.1012+179_1012+180insCGCCC
ENST00000696562.1:c.1012+179_1012+180insCGCCC	ENSP00000512720.1:n.1012+179_1012+180insCGCCC
ENST00000412585.7:c.1012+179_1012+180insCGCCC MANE Select	ENSP00000399168.2:n.1012+179_1012+180insCGCCC
ENST00000640094.1:c.89-263_89-262insCGCCC	ENSP00000491275.1:n.89-263_89-262insCGCCC
ENST00000412585.6:c.1012+179_1012+180insCGCCC	ENSP00000399168.2:n.1012+179_1012+180insCGCCC
ENST00000497377.5:n.149_150insCGCCC
NM_005514.6:c.1012+179_1012+180insCGCCC	NP_005505.2:n.1012+179_1012+180insCGCCC
XM_011514556.1:c.1045+179_1045+180insCGCCC	XP_011512858.1:n.1045+179_1045+180insCGCCC
XM_011514557.1:c.896-263_896-262insCGCCC	XP_011512859.1:n.896-263_896-262insCGCCC
XR_926175.1:n.1451+179_1451+180insCGCCC
NM_005514.7:c.1012+179_1012+180insCGCCC	NP_005505.2:n.1012+179_1012+180insCGCCC
NM_005514.8:c.1012+179_1012+180insCGCCC MANE Select	NP_005505.2:n.1012+179_1012+180insCGCCC