Canonical Allele Identifier: CA1619116922

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354436_31354439delinsCCAG , CM000668.2:g.31354436_31354439delinsCCAG	GRCh38
NC_000006.11:g.31322213_31322216delinsCCAG , CM000668.1:g.31322213_31322216delinsCCAG	GRCh37
NC_000006.10:g.31430192_31430195delinsCCAG	NCBI36
NG_023187.1:g.7774_7777delinsCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3140+40_3140+43delinsCTGG
ENST00000481849.6:n.3100+40_3100+43delinsCTGG
ENST00000497377.6:n.3007+40_3007+43delinsCTGG
ENST00000696558.1:c.1162+40_1162+43delinsCTGG	ENSP00000512716.1:n.1162+40_1162+43delinsCTGG
ENST00000696559.1:c.*4+40_*4+43delinsCTGG	ENSP00000512717.1:n.*4+40_*4+43delinsCTGG
ENST00000696560.1:c.*4+40_*4+43delinsCTGG	ENSP00000512718.1:n.*4+40_*4+43delinsCTGG
ENST00000696561.1:c.*4+40_*4+43delinsCTGG	ENSP00000512719.1:n.*4+40_*4+43delinsCTGG
ENST00000696562.1:c.*4+40_*4+43delinsCTGG	ENSP00000512720.1:n.*4+40_*4+43delinsCTGG
ENST00000412585.7:c.*4+40_*4+43delinsCTGG MANE Select	ENSP00000399168.2:n.*4+40_*4+43delinsCTGG
ENST00000412585.6:c.*4+40_*4+43delinsCTGG	ENSP00000399168.2:n.*4+40_*4+43delinsCTGG
ENST00000481849.5:n.328+40_328+43delinsCTGG
ENST00000497377.5:n.492+40_492+43delinsCTGG
NM_005514.6:c.*4+40_*4+43delinsCTGG	NP_005505.2:n.*4+40_*4+43delinsCTGG
XM_011514556.1:c.*4+40_*4+43delinsCTGG	XP_011512858.1:n.*4+40_*4+43delinsCTGG
XM_011514557.1:c.*4+40_*4+43delinsCTGG	XP_011512859.1:n.*4+40_*4+43delinsCTGG
XR_926175.1:n.1532+40_1532+43delinsCTGG
NM_005514.7:c.*4+40_*4+43delinsCTGG	NP_005505.2:n.*4+40_*4+43delinsCTGG
NM_005514.8:c.*4+40_*4+43delinsCTGG MANE Select	NP_005505.2:n.*4+40_*4+43delinsCTGG