Canonical Allele Identifier: CA1619112845

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356715_31356716delinsGC , CM000668.2:g.31356715_31356716delinsGC	GRCh38
NC_000006.11:g.31324492_31324493delinsGC , CM000668.1:g.31324492_31324493delinsGC	GRCh37
NC_000006.10:g.31432471_31432472delinsGC	NCBI36
NG_023187.1:g.5497_5498delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1788_1789delinsGC
ENST00000481849.6:n.1788_1789delinsGC
ENST00000497377.6:n.1788_1789delinsGC
ENST00000640094.2:c.315_316delinsGC	ENSP00000491275.2:p.Leu105=
ENST00000696558.1:c.315_316delinsGC	ENSP00000512716.1:p.Leu105=
ENST00000696559.1:c.315_316delinsGC	ENSP00000512717.1:p.Leu105=
ENST00000696560.1:c.315_316delinsGC	ENSP00000512718.1:p.Leu105=
ENST00000696561.1:c.315_316delinsGC	ENSP00000512719.1:p.Leu105=
ENST00000696562.1:c.315_316delinsGC	ENSP00000512720.1:p.Leu105=
ENST00000412585.7:c.315_316delinsGC MANE Select	ENSP00000399168.2:p.Leu105=
ENST00000412585.6:c.315_316delinsGC	ENSP00000399168.2:p.Leu105=
ENST00000434333.1:c.348_349delinsGC	ENSP00000405931.1:p.Leu116=
ENST00000474381.1:n.190_191delinsGC
ENST00000498007.1:n.336_337delinsGC
ENST00000603274.1:n.69_70delinsGC
NM_005514.6:c.315_316delinsGC	NP_005505.2:p.Leu105=
XM_011514556.1:c.348_349delinsGC	XP_011512858.1:p.Leu116=
XM_011514557.1:c.315_316delinsGC	XP_011512859.1:p.Leu105=
XR_926175.1:n.325_326delinsGC
NM_005514.7:c.315_316delinsGC	NP_005505.2:p.Leu105=
NM_005514.8:c.315_316delinsGC MANE Select	NP_005505.2:p.Leu105=