Canonical Allele Identifier: CA407998538

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610937A>C (hg19) ; chr20:g.1630291A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630291A>C , CM000682.2:g.1630291A>C	GRCh38
NC_000020.10:g.1610937A>C , CM000682.1:g.1610937A>C	GRCh37
NC_000020.9:g.1558937A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.764T>G	ENSP00000216927.4:p.Leu255Arg
ENST00000303415.7:c.1097T>G MANE Select	ENSP00000305529.3:p.Leu366Arg
ENST00000344103.8:c.446T>G	ENSP00000342759.4:p.Leu149Arg
ENST00000381580.5:c.998T>G	ENSP00000370992.1:p.Leu333Arg
ENST00000381583.6:c.764T>G	ENSP00000370995.2:p.Leu255Arg
ENST00000478145.6:n.158T>G
ENST00000497407.2:n.246T>G
NM_001039508.1:c.764T>G	NP_001034597.1:p.Leu255Arg
NM_018556.3:c.1097T>G	NP_061026.2:p.Leu366Arg
NM_080816.2:c.446T>G	NP_543006.2:p.Leu149Arg
XM_005260749.2:c.779T>G	XP_005260806.1:p.Leu260Arg
XM_011529286.1:c.998T>G	XP_011527588.1:p.Leu333Arg
XM_005260749.4:c.779T>G	XP_005260806.1:p.Leu260Arg
XM_011529286.2:c.998T>G	XP_011527588.1:p.Leu333Arg
NM_018556.4:c.1097T>G MANE Select	NP_061026.2:p.Leu366Arg
NM_080816.3:c.446T>G	NP_543006.2:p.Leu149Arg
NM_001039508.2:c.764T>G	NP_001034597.1:p.Leu255Arg