Canonical Allele Identifier: CA2677957669

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356745-G-GTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356746_31356747insTT , CM000668.2:g.31356746_31356747insTT	GRCh38
NC_000006.11:g.31324523_31324524insTT , CM000668.1:g.31324523_31324524insTT	GRCh37
NC_000006.10:g.31432502_31432503insTT	NCBI36
NG_023187.1:g.5467_5468insAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1758_1759insAA
ENST00000481849.6:n.1758_1759insAA
ENST00000497377.6:n.1758_1759insAA
ENST00000640094.2:c.285_286insAA	ENSP00000491275.2:p.Gln96AsnfsTer?
ENST00000696558.1:c.285_286insAA	ENSP00000512716.1:p.Gln96AsnfsTer?
ENST00000696559.1:c.285_286insAA	ENSP00000512717.1:p.Gln96AsnfsTer?
ENST00000696560.1:c.285_286insAA	ENSP00000512718.1:p.Gln96AsnfsTer?
ENST00000696561.1:c.285_286insAA	ENSP00000512719.1:p.Gln96AsnfsTer?
ENST00000696562.1:c.285_286insAA	ENSP00000512720.1:p.Gln96AsnfsTer?
ENST00000412585.7:c.285_286insAA MANE Select	ENSP00000399168.2:p.Gln96AsnfsTer?
ENST00000412585.6:c.285_286insAA	ENSP00000399168.2:p.Gln96AsnfsTer?
ENST00000434333.1:c.318_319insAA	ENSP00000405931.1:p.Gln107AsnfsTer?
ENST00000474381.1:n.160_161insAA
ENST00000498007.1:n.306_307insAA
ENST00000603274.1:n.100_101insTT
NM_005514.6:c.285_286insAA	NP_005505.2:p.Gln96AsnfsTer?
XM_011514556.1:c.318_319insAA	XP_011512858.1:p.Gln107AsnfsTer?
XM_011514557.1:c.285_286insAA	XP_011512859.1:p.Gln96AsnfsTer?
XR_926175.1:n.295_296insAA
NM_005514.7:c.285_286insAA	NP_005505.2:p.Gln96AsnfsTer?
NM_005514.8:c.285_286insAA MANE Select	NP_005505.2:p.Gln96AsnfsTer?