Canonical Allele Identifier: CA2554363378

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356276_31356277insGCC , CM000668.2:g.31356276_31356277insGCC	GRCh38
NC_000006.11:g.31324053_31324054insGCC , CM000668.1:g.31324053_31324054insGCC	GRCh37
NC_000006.10:g.31432032_31432033insGCC	NCBI36
NG_023187.1:g.5937_5938insGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1983_1984insGCG
ENST00000481849.6:n.1983_1984insGCG
ENST00000497377.6:n.1983_1984insGCG
ENST00000640094.2:c.510_511insGCG	ENSP00000491275.2:p.Lys170_Trp171insAla
ENST00000696558.1:c.510_511insGCG	ENSP00000512716.1:p.Lys170_Trp171insAla
ENST00000696559.1:c.510_511insGCG	ENSP00000512717.1:p.Lys170_Trp171insAla
ENST00000696560.1:c.510_511insGCG	ENSP00000512718.1:p.Lys170_Trp171insAla
ENST00000696561.1:c.510_511insGCG	ENSP00000512719.1:p.Lys170_Trp171insAla
ENST00000696562.1:c.510_511insGCG	ENSP00000512720.1:p.Lys170_Trp171insAla
ENST00000412585.7:c.510_511insGCG MANE Select	ENSP00000399168.2:p.Lys170_Trp171insAla
ENST00000412585.6:c.510_511insGCG	ENSP00000399168.2:p.Lys170_Trp171insAla
ENST00000434333.1:c.543_544insGCG	ENSP00000405931.1:p.Lys181_Trp182insAla
ENST00000474381.1:n.385_386insGCG
ENST00000498007.1:n.776_777insGCG
NM_005514.6:c.510_511insGCG	NP_005505.2:p.Lys170_Trp171insAla
XM_011514556.1:c.543_544insGCG	XP_011512858.1:p.Lys181_Trp182insAla
XM_011514557.1:c.510_511insGCG	XP_011512859.1:p.Lys170_Trp171insAla
XR_926175.1:n.520_521insGCG
NM_005514.7:c.510_511insGCG	NP_005505.2:p.Lys170_Trp171insAla
NM_005514.8:c.510_511insGCG MANE Select	NP_005505.2:p.Lys170_Trp171insAla