Canonical Allele Identifier: CA2770503828

Gene: HLA-B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356690del , CM000668.2:g.31356690del	GRCh38
NC_000006.11:g.31324467del , CM000668.1:g.31324467del	GRCh37
NC_000006.10:g.31432446del	NCBI36
NG_023187.1:g.5524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1815del
ENST00000481849.6:n.1815del
ENST00000497377.6:n.1815del
ENST00000640094.2:c.342del	ENSP00000491275.2:p.Ser116LeufsTer?
ENST00000696558.1:c.342del	ENSP00000512716.1:p.Ser116LeufsTer?
ENST00000696559.1:c.342del	ENSP00000512717.1:p.Ser116LeufsTer?
ENST00000696560.1:c.342del	ENSP00000512718.1:p.Ser116LeufsTer?
ENST00000696561.1:c.342del	ENSP00000512719.1:p.Ser116LeufsTer?
ENST00000696562.1:c.342del	ENSP00000512720.1:p.Ser116LeufsTer?
ENST00000412585.7:c.342del MANE Select	ENSP00000399168.2:p.Ser116LeufsTer?
ENST00000412585.6:c.342del	ENSP00000399168.2:p.Ser116LeufsTer?
ENST00000434333.1:c.375del	ENSP00000405931.1:p.Ser127LeufsTer?
ENST00000474381.1:n.217del
ENST00000498007.1:n.363del
ENST00000603274.1:n.44del
NM_005514.6:c.342del	NP_005505.2:p.Ser116LeufsTer?
XM_011514556.1:c.375del	XP_011512858.1:p.Ser127LeufsTer?
XM_011514557.1:c.342del	XP_011512859.1:p.Ser116LeufsTer?
XR_926175.1:n.352del
NM_005514.7:c.342del	NP_005505.2:p.Ser116LeufsTer?
NM_005514.8:c.342del MANE Select	NP_005505.2:p.Ser116LeufsTer?