Canonical Allele Identifier: CA407998545

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610940G>C (hg19) ; chr20:g.1630294G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630294G>C , CM000682.2:g.1630294G>C	GRCh38
NC_000020.10:g.1610940G>C , CM000682.1:g.1610940G>C	GRCh37
NC_000020.9:g.1558940G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.761C>G	ENSP00000216927.4:p.Ser254Cys
ENST00000303415.7:c.1094C>G MANE Select	ENSP00000305529.3:p.Ser365Cys
ENST00000344103.8:c.443C>G	ENSP00000342759.4:p.Ser148Cys
ENST00000381580.5:c.995C>G	ENSP00000370992.1:p.Ser332Cys
ENST00000381583.6:c.761C>G	ENSP00000370995.2:p.Ser254Cys
ENST00000478145.6:n.155C>G
ENST00000497407.2:n.243C>G
NM_001039508.1:c.761C>G	NP_001034597.1:p.Ser254Cys
NM_018556.3:c.1094C>G	NP_061026.2:p.Ser365Cys
NM_080816.2:c.443C>G	NP_543006.2:p.Ser148Cys
XM_005260749.2:c.776C>G	XP_005260806.1:p.Ser259Cys
XM_011529286.1:c.995C>G	XP_011527588.1:p.Ser332Cys
XM_005260749.4:c.776C>G	XP_005260806.1:p.Ser259Cys
XM_011529286.2:c.995C>G	XP_011527588.1:p.Ser332Cys
NM_018556.4:c.1094C>G MANE Select	NP_061026.2:p.Ser365Cys
NM_080816.3:c.443C>G	NP_543006.2:p.Ser148Cys
NM_001039508.2:c.761C>G	NP_001034597.1:p.Ser254Cys