Canonical Allele Identifier: CA2539537797

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355219del , CM000668.2:g.31355219del	GRCh38
NC_000006.11:g.31322996del , CM000668.1:g.31322996del	GRCh37
NC_000006.10:g.31430975del	NCBI36
NG_023187.1:g.6994del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2947del
ENST00000481849.6:n.2466del
ENST00000497377.6:n.2373del
ENST00000640094.2:c.895+98del	ENSP00000491275.2:n.895+98del
ENST00000696558.1:c.969del	ENSP00000512716.1:n.969del
ENST00000696559.1:c.900del	ENSP00000512717.1:p.Ser301LeufsTer18
ENST00000696560.1:c.900del	ENSP00000512718.1:p.Ser301LeufsTer18
ENST00000696561.1:c.900del	ENSP00000512719.1:p.Ser301LeufsTer18
ENST00000696562.1:c.900del	ENSP00000512720.1:p.Ser301LeufsTer18
ENST00000412585.7:c.900del MANE Select	ENSP00000399168.2:p.Ser301LeufsTer18
ENST00000640094.1:c.88+98del	ENSP00000491275.1:n.88+98del
ENST00000412585.6:c.900del	ENSP00000399168.2:p.Ser301LeufsTer18
ENST00000463574.1:n.491del
NM_005514.6:c.900del	NP_005505.2:p.Ser301LeufsTer18
XM_011514556.1:c.933del	XP_011512858.1:p.Ser312LeufsTer18
XM_011514557.1:c.895+98del	XP_011512859.1:n.895+98del
XR_926175.1:n.1339del
NM_005514.7:c.900del	NP_005505.2:p.Ser301LeufsTer18
NM_005514.8:c.900del MANE Select	NP_005505.2:p.Ser301LeufsTer18