Canonical Allele Identifier: CA2345733444

Gene: SIRPG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630227G= , CM000682.2:g.1630227G=	GRCh38
NC_000020.10:g.1610873G= , CM000682.1:g.1610873G=	GRCh37
NC_000020.9:g.1558873G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.828C=	ENSP00000216927.4:p.Thr276=
ENST00000303415.7:c.1161C= MANE Select	ENSP00000305529.3:p.Thr387=
ENST00000344103.8:c.510C=	ENSP00000342759.4:p.Thr170=
ENST00000381580.5:c.1062C=	ENSP00000370992.1:p.Thr354=
ENST00000381583.6:c.828C=	ENSP00000370995.2:p.Thr276=
ENST00000478145.6:n.222C=
ENST00000497407.2:n.310C=
NM_001039508.1:c.828C=	NP_001034597.1:p.Thr276=
NM_018556.3:c.1161C=	NP_061026.2:p.Thr387=
NM_080816.2:c.510C=	NP_543006.2:p.Thr170=
XM_005260749.2:c.843C=	XP_005260806.1:p.Thr281=
XM_011529286.1:c.1062C=	XP_011527588.1:p.Thr354=
XM_005260749.4:c.843C=	XP_005260806.1:p.Thr281=
XM_011529286.2:c.1062C=	XP_011527588.1:p.Thr354=
NM_018556.4:c.1161C= MANE Select	NP_061026.2:p.Thr387=
NM_080816.3:c.510C=	NP_543006.2:p.Thr170=
NM_001039508.2:c.828C=	NP_001034597.1:p.Thr276=