Canonical Allele Identifier: CA2770503536

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31354504_31354507del , CM000668.2:g.31354504_31354507del	GRCh38
NC_000006.11:g.31322281_31322284del , CM000668.1:g.31322281_31322284del	GRCh37
NC_000006.10:g.31430260_31430263del	NCBI36
NG_023187.1:g.7706_7709del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3112_3115del
ENST00000481849.6:n.3072_3075del
ENST00000497377.6:n.2979_2982del
ENST00000640094.2:c.948_951del	ENSP00000491275.2:p.Ser317MetfsTer?
ENST00000696558.1:c.1134_1137del	ENSP00000512716.1:n.1134_1137del
ENST00000696559.1:c.1065_1068del	ENSP00000512717.1:p.Ser356MetfsTer15
ENST00000696560.1:c.1065_1068del	ENSP00000512718.1:p.Ser356MetfsTer15
ENST00000696561.1:c.1065_1068del	ENSP00000512719.1:p.Ser356MetfsTer15
ENST00000696562.1:c.1065_1068del	ENSP00000512720.1:p.Ser356MetfsTer15
ENST00000412585.7:c.1065_1068del MANE Select	ENSP00000399168.2:p.Ser356MetfsTer15
ENST00000640094.1:c.141_144del	ENSP00000491275.1:p.Gly47=
ENST00000412585.6:c.1065_1068del	ENSP00000399168.2:p.Ser356MetfsTer15
ENST00000481849.5:n.300_303del
ENST00000497377.5:n.464_467del
NM_005514.6:c.1065_1068del	NP_005505.2:p.Ser356MetfsTer15
XM_011514556.1:c.1098_1101del	XP_011512858.1:p.Ser367MetfsTer15
XM_011514557.1:c.948_951del	XP_011512859.1:p.Ser317MetfsTer15
XR_926175.1:n.1504_1507del
NM_005514.7:c.1065_1068del	NP_005505.2:p.Ser356MetfsTer15
NM_005514.8:c.1065_1068del MANE Select	NP_005505.2:p.Ser356MetfsTer15