Canonical Allele Identifier: CA1619118215

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355146_31355152delinsCTCCGAT , CM000668.2:g.31355146_31355152delinsCTCCGAT	GRCh38
NC_000006.11:g.31322923_31322929delinsCTCCGAT , CM000668.1:g.31322923_31322929delinsCTCCGAT	GRCh37
NC_000006.10:g.31430902_31430908delinsCTCCGAT	NCBI36
NG_023187.1:g.7061_7067delinsATCGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3014_3020delinsATCGGAG
ENST00000481849.6:n.2533_2539delinsATCGGAG
ENST00000497377.6:n.2440_2446delinsATCGGAG
ENST00000640094.2:c.895+165_895+171delinsATCGGAG	ENSP00000491275.2:n.895+165_895+171delinsATCGGAG
ENST00000696558.1:c.1036_1042delinsATCGGAG	ENSP00000512716.1:n.1036_1042delinsATCGGAG
ENST00000696559.1:c.967_973delinsATCGGAG	ENSP00000512717.1:p.Ile323=
ENST00000696560.1:c.967_973delinsATCGGAG	ENSP00000512718.1:p.Ile323=
ENST00000696561.1:c.967_973delinsATCGGAG	ENSP00000512719.1:p.Ile323=
ENST00000696562.1:c.967_973delinsATCGGAG	ENSP00000512720.1:p.Ile323=
ENST00000412585.7:c.967_973delinsATCGGAG MANE Select	ENSP00000399168.2:p.Ile323=
ENST00000640094.1:c.88+165_88+171delinsATCGGAG	ENSP00000491275.1:n.88+165_88+171delinsATCGGAG
ENST00000412585.6:c.967_973delinsATCGGAG	ENSP00000399168.2:p.Ile323=
ENST00000463574.1:n.558_564delinsATCGGAG
NM_005514.6:c.967_973delinsATCGGAG	NP_005505.2:p.Ile323=
XM_011514556.1:c.1000_1006delinsATCGGAG	XP_011512858.1:p.Ile334=
XM_011514557.1:c.895+165_895+171delinsATCGGAG	XP_011512859.1:n.895+165_895+171delinsATCGGAG
XR_926175.1:n.1406_1412delinsATCGGAG
NM_005514.7:c.967_973delinsATCGGAG	NP_005505.2:p.Ile323=
NM_005514.8:c.967_973delinsATCGGAG MANE Select	NP_005505.2:p.Ile323=