Canonical Allele Identifier: CA2345733447

Gene: SIRPG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630231T= , CM000682.2:g.1630231T=	GRCh38
NC_000020.10:g.1610877T= , CM000682.1:g.1610877T=	GRCh37
NC_000020.9:g.1558877T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.824A=	ENSP00000216927.4:p.Lys275=
ENST00000303415.7:c.1157A= MANE Select	ENSP00000305529.3:p.Lys386=
ENST00000344103.8:c.506A=	ENSP00000342759.4:p.Lys169=
ENST00000381580.5:c.1058A=	ENSP00000370992.1:p.Lys353=
ENST00000381583.6:c.824A=	ENSP00000370995.2:p.Lys275=
ENST00000478145.6:n.218A=
ENST00000497407.2:n.306A=
NM_001039508.1:c.824A=	NP_001034597.1:p.Lys275=
NM_018556.3:c.1157A=	NP_061026.2:p.Lys386=
NM_080816.2:c.506A=	NP_543006.2:p.Lys169=
XM_005260749.2:c.839A=	XP_005260806.1:p.Lys280=
XM_011529286.1:c.1058A=	XP_011527588.1:p.Lys353=
XM_005260749.4:c.839A=	XP_005260806.1:p.Lys280=
XM_011529286.2:c.1058A=	XP_011527588.1:p.Lys353=
NM_018556.4:c.1157A= MANE Select	NP_061026.2:p.Lys386=
NM_080816.3:c.506A=	NP_543006.2:p.Lys169=
NM_001039508.2:c.824A=	NP_001034597.1:p.Lys275=