Canonical Allele Identifier: CA1619112891

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356720_31356730delinsTTCCGCAGGCT , CM000668.2:g.31356720_31356730delinsTTCCGCAGGCT	GRCh38
NC_000006.11:g.31324497_31324507delinsTTCCGCAGGCT , CM000668.1:g.31324497_31324507delinsTTCCGCAGGCT	GRCh37
NC_000006.10:g.31432476_31432486delinsTTCCGCAGGCT	NCBI36
NG_023187.1:g.5483_5493delinsAGCCTGCGGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1774_1784delinsAGCCTGCGGAA
ENST00000481849.6:n.1774_1784delinsAGCCTGCGGAA
ENST00000497377.6:n.1774_1784delinsAGCCTGCGGAA
ENST00000640094.2:c.301_311delinsAGCCTGCGGAA	ENSP00000491275.2:p.Ser101=
ENST00000696558.1:c.301_311delinsAGCCTGCGGAA	ENSP00000512716.1:p.Ser101=
ENST00000696559.1:c.301_311delinsAGCCTGCGGAA	ENSP00000512717.1:p.Ser101=
ENST00000696560.1:c.301_311delinsAGCCTGCGGAA	ENSP00000512718.1:p.Ser101=
ENST00000696561.1:c.301_311delinsAGCCTGCGGAA	ENSP00000512719.1:p.Ser101=
ENST00000696562.1:c.301_311delinsAGCCTGCGGAA	ENSP00000512720.1:p.Ser101=
ENST00000412585.7:c.301_311delinsAGCCTGCGGAA MANE Select	ENSP00000399168.2:p.Ser101=
ENST00000412585.6:c.301_311delinsAGCCTGCGGAA	ENSP00000399168.2:p.Ser101=
ENST00000434333.1:c.334_344delinsAGCCTGCGGAA	ENSP00000405931.1:p.Ser112=
ENST00000474381.1:n.176_186delinsAGCCTGCGGAA
ENST00000498007.1:n.322_332delinsAGCCTGCGGAA
ENST00000603274.1:n.74_84delinsTTCCGCAGGCT
NM_005514.6:c.301_311delinsAGCCTGCGGAA	NP_005505.2:p.Ser101=
XM_011514556.1:c.334_344delinsAGCCTGCGGAA	XP_011512858.1:p.Ser112=
XM_011514557.1:c.301_311delinsAGCCTGCGGAA	XP_011512859.1:p.Ser101=
XR_926175.1:n.311_321delinsAGCCTGCGGAA
NM_005514.7:c.301_311delinsAGCCTGCGGAA	NP_005505.2:p.Ser101=
NM_005514.8:c.301_311delinsAGCCTGCGGAA MANE Select	NP_005505.2:p.Ser101=