Canonical Allele Identifier: CA1087469469

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356751-G-GCT
• gnomAD v4: 6-31356751-G-GCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356751_31356752insCT , CM000668.2:g.31356751_31356752insCT	GRCh38
NC_000006.11:g.31324528_31324529insCT , CM000668.1:g.31324528_31324529insCT	GRCh37
NC_000006.10:g.31432507_31432508insCT	NCBI36
NG_023187.1:g.5461_5462insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1752_1753insAG
ENST00000481849.6:n.1752_1753insAG
ENST00000497377.6:n.1752_1753insAG
ENST00000640094.2:c.279_280insAG	ENSP00000491275.2:p.Gln94SerfsTer?
ENST00000696558.1:c.279_280insAG	ENSP00000512716.1:p.Gln94SerfsTer?
ENST00000696559.1:c.279_280insAG	ENSP00000512717.1:p.Gln94SerfsTer?
ENST00000696560.1:c.279_280insAG	ENSP00000512718.1:p.Gln94SerfsTer?
ENST00000696561.1:c.279_280insAG	ENSP00000512719.1:p.Gln94SerfsTer?
ENST00000696562.1:c.279_280insAG	ENSP00000512720.1:p.Gln94SerfsTer?
ENST00000412585.7:c.279_280insAG MANE Select	ENSP00000399168.2:p.Gln94SerfsTer?
ENST00000412585.6:c.279_280insAG	ENSP00000399168.2:p.Gln94SerfsTer?
ENST00000434333.1:c.312_313insAG	ENSP00000405931.1:p.Gln105SerfsTer?
ENST00000474381.1:n.154_155insAG
ENST00000498007.1:n.300_301insAG
ENST00000603274.1:n.105_106insCT
NM_005514.6:c.279_280insAG	NP_005505.2:p.Gln94SerfsTer?
XM_011514556.1:c.312_313insAG	XP_011512858.1:p.Gln105SerfsTer?
XM_011514557.1:c.279_280insAG	XP_011512859.1:p.Gln94SerfsTer?
XR_926175.1:n.289_290insAG
NM_005514.7:c.279_280insAG	NP_005505.2:p.Gln94SerfsTer?
NM_005514.8:c.279_280insAG MANE Select	NP_005505.2:p.Gln94SerfsTer?