Canonical Allele Identifier: CA449601296

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31322963_31322964insT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355186_31355187insT , CM000668.2:g.31355186_31355187insT	GRCh38
NC_000006.11:g.31322963_31322964insT , CM000668.1:g.31322963_31322964insT	GRCh37
NC_000006.10:g.31430942_31430943insT	NCBI36
NG_023187.1:g.7026_7027insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2979_2980insA
ENST00000481849.6:n.2498_2499insA
ENST00000497377.6:n.2405_2406insA
ENST00000640094.2:c.895+130_895+131insA	ENSP00000491275.2:n.895+130_895+131insA
ENST00000696558.1:c.1001_1002insA	ENSP00000512716.1:n.1001_1002insA
ENST00000696559.1:c.932_933insA	ENSP00000512717.1:p.Val312CysfsTer22
ENST00000696560.1:c.932_933insA	ENSP00000512718.1:p.Val312CysfsTer22
ENST00000696561.1:c.932_933insA	ENSP00000512719.1:p.Val312CysfsTer22
ENST00000696562.1:c.932_933insA	ENSP00000512720.1:p.Val312CysfsTer22
ENST00000412585.7:c.932_933insA MANE Select	ENSP00000399168.2:p.Val312CysfsTer22
ENST00000640094.1:c.88+130_88+131insA	ENSP00000491275.1:n.88+130_88+131insA
ENST00000412585.6:c.932_933insA	ENSP00000399168.2:p.Val312CysfsTer22
ENST00000463574.1:n.523_524insA
NM_005514.6:c.932_933insA	NP_005505.2:p.Val312CysfsTer22
XM_011514556.1:c.965_966insA	XP_011512858.1:p.Val323CysfsTer22
XM_011514557.1:c.895+130_895+131insA	XP_011512859.1:n.895+130_895+131insA
XR_926175.1:n.1371_1372insA
NM_005514.7:c.932_933insA	NP_005505.2:p.Val312CysfsTer22
NM_005514.8:c.932_933insA MANE Select	NP_005505.2:p.Val312CysfsTer22