Canonical Allele Identifier: CA1619119969

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356096_31356098delinsTCC , CM000668.2:g.31356096_31356098delinsTCC	GRCh38
NC_000006.11:g.31323873_31323875delinsTCC , CM000668.1:g.31323873_31323875delinsTCC	GRCh37
NC_000006.10:g.31431852_31431854delinsTCC	NCBI36
NG_023187.1:g.6115_6117delinsGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2161_2163delinsGGA
ENST00000481849.6:n.2092+69_2092+71delinsGGA
ENST00000497377.6:n.2092+69_2092+71delinsGGA
ENST00000640094.2:c.619+69_619+71delinsGGA	ENSP00000491275.2:n.619+69_619+71delinsGGA
ENST00000696558.1:c.619+69_619+71delinsGGA	ENSP00000512716.1:n.619+69_619+71delinsGGA
ENST00000696559.1:c.619+69_619+71delinsGGA	ENSP00000512717.1:n.619+69_619+71delinsGGA
ENST00000696560.1:c.619+69_619+71delinsGGA	ENSP00000512718.1:n.619+69_619+71delinsGGA
ENST00000696561.1:c.619+69_619+71delinsGGA	ENSP00000512719.1:n.619+69_619+71delinsGGA
ENST00000696562.1:c.619+69_619+71delinsGGA	ENSP00000512720.1:n.619+69_619+71delinsGGA
ENST00000412585.7:c.619+69_619+71delinsGGA MANE Select	ENSP00000399168.2:n.619+69_619+71delinsGGA
ENST00000412585.6:c.619+69_619+71delinsGGA	ENSP00000399168.2:n.619+69_619+71delinsGGA
ENST00000434333.1:c.652+69_652+71delinsGGA	ENSP00000405931.1:n.652+69_652+71delinsGGA
ENST00000474381.1:n.563_565delinsGGA
ENST00000498007.1:n.885+69_885+71delinsGGA
NM_005514.6:c.619+69_619+71delinsGGA	NP_005505.2:n.619+69_619+71delinsGGA
XM_011514556.1:c.652+69_652+71delinsGGA	XP_011512858.1:n.652+69_652+71delinsGGA
XM_011514557.1:c.619+69_619+71delinsGGA	XP_011512859.1:n.619+69_619+71delinsGGA
XR_926175.1:n.698_700delinsGGA
NM_005514.7:c.619+69_619+71delinsGGA	NP_005505.2:n.619+69_619+71delinsGGA
NM_005514.8:c.619+69_619+71delinsGGA MANE Select	NP_005505.2:n.619+69_619+71delinsGGA