Canonical Allele Identifier: CA2838643836

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356398_31356399insGGGCCCCA , CM000668.2:g.31356398_31356399insGGGCCCCA	GRCh38
NC_000006.11:g.31324175_31324176insGGGCCCCA , CM000668.1:g.31324175_31324176insGGGCCCCA	GRCh37
NC_000006.10:g.31432154_31432155insGGGCCCCA	NCBI36
NG_023187.1:g.5814_5815insTGGGGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1860_1861insTGGGGCCC
ENST00000481849.6:n.1860_1861insTGGGGCCC
ENST00000497377.6:n.1860_1861insTGGGGCCC
ENST00000640094.2:c.387_388insTGGGGCCC	ENSP00000491275.2:p.Asp130TrpfsTer24
ENST00000696558.1:c.387_388insTGGGGCCC	ENSP00000512716.1:p.Asp130TrpfsTer24
ENST00000696559.1:c.387_388insTGGGGCCC	ENSP00000512717.1:p.Asp130TrpfsTer24
ENST00000696560.1:c.387_388insTGGGGCCC	ENSP00000512718.1:p.Asp130TrpfsTer24
ENST00000696561.1:c.387_388insTGGGGCCC	ENSP00000512719.1:p.Asp130TrpfsTer24
ENST00000696562.1:c.387_388insTGGGGCCC	ENSP00000512720.1:p.Asp130TrpfsTer24
ENST00000412585.7:c.387_388insTGGGGCCC MANE Select	ENSP00000399168.2:p.Asp130TrpfsTer24
ENST00000412585.6:c.387_388insTGGGGCCC	ENSP00000399168.2:p.Asp130TrpfsTer24
ENST00000434333.1:c.420_421insTGGGGCCC	ENSP00000405931.1:p.Asp141TrpfsTer24
ENST00000474381.1:n.262_263insTGGGGCCC
ENST00000498007.1:n.653_654insTGGGGCCC
NM_005514.6:c.387_388insTGGGGCCC	NP_005505.2:p.Asp130TrpfsTer24
XM_011514556.1:c.420_421insTGGGGCCC	XP_011512858.1:p.Asp141TrpfsTer24
XM_011514557.1:c.387_388insTGGGGCCC	XP_011512859.1:p.Asp130TrpfsTer24
XR_926175.1:n.397_398insTGGGGCCC
NM_005514.7:c.387_388insTGGGGCCC	NP_005505.2:p.Asp130TrpfsTer24
NM_005514.8:c.387_388insTGGGGCCC MANE Select	NP_005505.2:p.Asp130TrpfsTer24