Canonical Allele Identifier: CA509367579

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610903G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630257G>C , CM000682.2:g.1630257G>C	GRCh38
NC_000020.10:g.1610903G>C , CM000682.1:g.1610903G>C	GRCh37
NC_000020.9:g.1558903G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.798C>G	ENSP00000216927.4:p.Gly266=
ENST00000303415.7:c.1131C>G MANE Select	ENSP00000305529.3:p.Gly377=
ENST00000344103.8:c.480C>G	ENSP00000342759.4:p.Gly160=
ENST00000381580.5:c.1032C>G	ENSP00000370992.1:p.Gly344=
ENST00000381583.6:c.798C>G	ENSP00000370995.2:p.Gly266=
ENST00000478145.6:n.192C>G
ENST00000497407.2:n.280C>G
NM_001039508.1:c.798C>G	NP_001034597.1:p.Gly266=
NM_018556.3:c.1131C>G	NP_061026.2:p.Gly377=
NM_080816.2:c.480C>G	NP_543006.2:p.Gly160=
XM_005260749.2:c.813C>G	XP_005260806.1:p.Gly271=
XM_011529286.1:c.1032C>G	XP_011527588.1:p.Gly344=
XM_005260749.4:c.813C>G	XP_005260806.1:p.Gly271=
XM_011529286.2:c.1032C>G	XP_011527588.1:p.Gly344=
NM_018556.4:c.1131C>G MANE Select	NP_061026.2:p.Gly377=
NM_080816.3:c.480C>G	NP_543006.2:p.Gly160=
NM_001039508.2:c.798C>G	NP_001034597.1:p.Gly266=