Canonical Allele Identifier: CA2677957668

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356745-G-GTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356746_31356747insAT , CM000668.2:g.31356746_31356747insAT	GRCh38
NC_000006.11:g.31324523_31324524insAT , CM000668.1:g.31324523_31324524insAT	GRCh37
NC_000006.10:g.31432502_31432503insAT	NCBI36
NG_023187.1:g.5467_5468insTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1758_1759insTA
ENST00000481849.6:n.1758_1759insTA
ENST00000497377.6:n.1758_1759insTA
ENST00000640094.2:c.285_286insTA	ENSP00000491275.2:p.Gln96TyrfsTer?
ENST00000696558.1:c.285_286insTA	ENSP00000512716.1:p.Gln96TyrfsTer?
ENST00000696559.1:c.285_286insTA	ENSP00000512717.1:p.Gln96TyrfsTer?
ENST00000696560.1:c.285_286insTA	ENSP00000512718.1:p.Gln96TyrfsTer?
ENST00000696561.1:c.285_286insTA	ENSP00000512719.1:p.Gln96TyrfsTer?
ENST00000696562.1:c.285_286insTA	ENSP00000512720.1:p.Gln96TyrfsTer?
ENST00000412585.7:c.285_286insTA MANE Select	ENSP00000399168.2:p.Gln96TyrfsTer?
ENST00000412585.6:c.285_286insTA	ENSP00000399168.2:p.Gln96TyrfsTer?
ENST00000434333.1:c.318_319insTA	ENSP00000405931.1:p.Gln107TyrfsTer?
ENST00000474381.1:n.160_161insTA
ENST00000498007.1:n.306_307insTA
ENST00000603274.1:n.100_101insAT
NM_005514.6:c.285_286insTA	NP_005505.2:p.Gln96TyrfsTer?
XM_011514556.1:c.318_319insTA	XP_011512858.1:p.Gln107TyrfsTer?
XM_011514557.1:c.285_286insTA	XP_011512859.1:p.Gln96TyrfsTer?
XR_926175.1:n.295_296insTA
NM_005514.7:c.285_286insTA	NP_005505.2:p.Gln96TyrfsTer?
NM_005514.8:c.285_286insTA MANE Select	NP_005505.2:p.Gln96TyrfsTer?