Canonical Allele Identifier: CA1619113574

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356887_31356889delinsTGA , CM000668.2:g.31356887_31356889delinsTGA	GRCh38
NC_000006.11:g.31324664_31324666delinsTGA , CM000668.1:g.31324664_31324666delinsTGA	GRCh37
NC_000006.10:g.31432643_31432645delinsTGA	NCBI36
NG_023187.1:g.5324_5326delinsTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1615_1617delinsTCA
ENST00000481849.6:n.1615_1617delinsTCA
ENST00000497377.6:n.1615_1617delinsTCA
ENST00000640094.2:c.142_144delinsTCA	ENSP00000491275.2:p.Ser48=
ENST00000696558.1:c.142_144delinsTCA	ENSP00000512716.1:p.Ser48=
ENST00000696559.1:c.142_144delinsTCA	ENSP00000512717.1:p.Ser48=
ENST00000696560.1:c.142_144delinsTCA	ENSP00000512718.1:p.Ser48=
ENST00000696561.1:c.142_144delinsTCA	ENSP00000512719.1:p.Ser48=
ENST00000696562.1:c.142_144delinsTCA	ENSP00000512720.1:p.Ser48=
ENST00000412585.7:c.142_144delinsTCA MANE Select	ENSP00000399168.2:p.Ser48=
ENST00000412585.6:c.142_144delinsTCA	ENSP00000399168.2:p.Ser48=
ENST00000434333.1:c.175_177delinsTCA	ENSP00000405931.1:p.Ser59=
ENST00000474381.1:n.17_19delinsTCA
ENST00000498007.1:n.163_165delinsTCA
ENST00000603274.1:n.241_243delinsTGA
NM_005514.6:c.142_144delinsTCA	NP_005505.2:p.Ser48=
XM_011514556.1:c.175_177delinsTCA	XP_011512858.1:p.Ser59=
XM_011514557.1:c.142_144delinsTCA	XP_011512859.1:p.Ser48=
XR_926175.1:n.152_154delinsTCA
NM_005514.7:c.142_144delinsTCA	NP_005505.2:p.Ser48=
NM_005514.8:c.142_144delinsTCA MANE Select	NP_005505.2:p.Ser48=