Canonical Allele Identifier: CA1619112146

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356431_31356433delinsGGG , CM000668.2:g.31356431_31356433delinsGGG	GRCh38
NC_000006.11:g.31324208_31324210delinsGGG , CM000668.1:g.31324208_31324210delinsGGG	GRCh37
NC_000006.10:g.31432187_31432189delinsGGG	NCBI36
NG_023187.1:g.5780_5782delinsCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1826_1828delinsCCC
ENST00000481849.6:n.1826_1828delinsCCC
ENST00000497377.6:n.1826_1828delinsCCC
ENST00000640094.2:c.353_355delinsCCC	ENSP00000491275.2:p.Thr118=
ENST00000696558.1:c.353_355delinsCCC	ENSP00000512716.1:p.Thr118=
ENST00000696559.1:c.353_355delinsCCC	ENSP00000512717.1:p.Thr118=
ENST00000696560.1:c.353_355delinsCCC	ENSP00000512718.1:p.Thr118=
ENST00000696561.1:c.353_355delinsCCC	ENSP00000512719.1:p.Thr118=
ENST00000696562.1:c.353_355delinsCCC	ENSP00000512720.1:p.Thr118=
ENST00000412585.7:c.353_355delinsCCC MANE Select	ENSP00000399168.2:p.Thr118=
ENST00000412585.6:c.353_355delinsCCC	ENSP00000399168.2:p.Thr118=
ENST00000434333.1:c.386_388delinsCCC	ENSP00000405931.1:p.Thr129=
ENST00000474381.1:n.228_230delinsCCC
ENST00000498007.1:n.619_621delinsCCC
NM_005514.6:c.353_355delinsCCC	NP_005505.2:p.Thr118=
XM_011514556.1:c.386_388delinsCCC	XP_011512858.1:p.Thr129=
XM_011514557.1:c.353_355delinsCCC	XP_011512859.1:p.Thr118=
XR_926175.1:n.363_365delinsCCC
NM_005514.7:c.353_355delinsCCC	NP_005505.2:p.Thr118=
NM_005514.8:c.353_355delinsCCC MANE Select	NP_005505.2:p.Thr118=