Canonical Allele Identifier: CA1619116325

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31353923_31353927delinsCTTAT , CM000668.2:g.31353923_31353927delinsCTTAT	GRCh38
NC_000006.11:g.31321700_31321704delinsCTTAT , CM000668.1:g.31321700_31321704delinsCTTAT	GRCh37
NC_000006.10:g.31429679_31429683delinsCTTAT	NCBI36
NG_023187.1:g.8286_8290delinsATAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3510_3514delinsATAAG
ENST00000481849.6:n.3470_3474delinsATAAG
ENST00000497377.6:n.3377_3381delinsATAAG
ENST00000696558.1:c.1532_1536delinsATAAG	ENSP00000512716.1:n.1532_1536delinsATAAG
ENST00000696559.1:c.*374_*378delinsATAAG	ENSP00000512717.1:n.*374_*378delinsATAAG
ENST00000696560.1:c.*374_*378delinsATAAG	ENSP00000512718.1:n.*374_*378delinsATAAG
ENST00000696561.1:c.*374_*378delinsATAAG	ENSP00000512719.1:n.*374_*378delinsATAAG
ENST00000696562.1:c.*374_*378delinsATAAG	ENSP00000512720.1:n.*374_*378delinsATAAG
ENST00000412585.7:c.*374_*378delinsATAAG MANE Select	ENSP00000399168.2:n.*374_*378delinsATAAG
ENST00000412585.6:c.*374_*378delinsATAAG	ENSP00000399168.2:n.*374_*378delinsATAAG
ENST00000481849.5:n.698_702delinsATAAG
ENST00000497377.5:n.862_866delinsATAAG
NM_005514.6:c.*374_*378delinsATAAG	NP_005505.2:n.*374_*378delinsATAAG
XM_011514556.1:c.*374_*378delinsATAAG	XP_011512858.1:n.*374_*378delinsATAAG
XM_011514557.1:c.*374_*378delinsATAAG	XP_011512859.1:n.*374_*378delinsATAAG
XR_926175.1:n.1902_1906delinsATAAG
NM_005514.7:c.*374_*378delinsATAAG	NP_005505.2:n.*374_*378delinsATAAG
NM_005514.8:c.*374_*378delinsATAAG MANE Select	NP_005505.2:n.*374_*378delinsATAAG