Canonical Allele Identifier: CA407998547

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610941A>C (hg19) ; chr20:g.1630295A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630295A>C , CM000682.2:g.1630295A>C	GRCh38
NC_000020.10:g.1610941A>C , CM000682.1:g.1610941A>C	GRCh37
NC_000020.9:g.1558941A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.760T>G	ENSP00000216927.4:p.Ser254Ala
ENST00000303415.7:c.1093T>G MANE Select	ENSP00000305529.3:p.Ser365Ala
ENST00000344103.8:c.442T>G	ENSP00000342759.4:p.Ser148Ala
ENST00000381580.5:c.994T>G	ENSP00000370992.1:p.Ser332Ala
ENST00000381583.6:c.760T>G	ENSP00000370995.2:p.Ser254Ala
ENST00000478145.6:n.154T>G
ENST00000497407.2:n.242T>G
NM_001039508.1:c.760T>G	NP_001034597.1:p.Ser254Ala
NM_018556.3:c.1093T>G	NP_061026.2:p.Ser365Ala
NM_080816.2:c.442T>G	NP_543006.2:p.Ser148Ala
XM_005260749.2:c.775T>G	XP_005260806.1:p.Ser259Ala
XM_011529286.1:c.994T>G	XP_011527588.1:p.Ser332Ala
XM_005260749.4:c.775T>G	XP_005260806.1:p.Ser259Ala
XM_011529286.2:c.994T>G	XP_011527588.1:p.Ser332Ala
NM_018556.4:c.1093T>G MANE Select	NP_061026.2:p.Ser365Ala
NM_080816.3:c.442T>G	NP_543006.2:p.Ser148Ala
NM_001039508.2:c.760T>G	NP_001034597.1:p.Ser254Ala