Canonical Allele Identifier: CA407998549

Gene: SIRPG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.760T>A	ENSP00000216927.4:p.Ser254Thr
ENST00000303415.7:c.1093T>A MANE Select	ENSP00000305529.3:p.Ser365Thr
ENST00000344103.8:c.442T>A	ENSP00000342759.4:p.Ser148Thr
ENST00000381580.5:c.994T>A	ENSP00000370992.1:p.Ser332Thr
ENST00000381583.6:c.760T>A	ENSP00000370995.2:p.Ser254Thr
ENST00000478145.6:n.154T>A
ENST00000497407.2:n.242T>A
NM_001039508.1:c.760T>A	NP_001034597.1:p.Ser254Thr
NM_018556.3:c.1093T>A	NP_061026.2:p.Ser365Thr
NM_080816.2:c.442T>A	NP_543006.2:p.Ser148Thr
XM_005260749.2:c.775T>A	XP_005260806.1:p.Ser259Thr
XM_011529286.1:c.994T>A	XP_011527588.1:p.Ser332Thr
XM_005260749.4:c.775T>A	XP_005260806.1:p.Ser259Thr
XM_011529286.2:c.994T>A	XP_011527588.1:p.Ser332Thr
NM_018556.4:c.1093T>A MANE Select	NP_061026.2:p.Ser365Thr
NM_080816.3:c.442T>A	NP_543006.2:p.Ser148Thr
NM_001039508.2:c.760T>A	NP_001034597.1:p.Ser254Thr