Canonical Allele Identifier: CA407998502

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630271-C-T
• MyVariant Identifiers: chr20:g.1610917C>T (hg19) ; chr20:g.1630271C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630271C>T , CM000682.2:g.1630271C>T	GRCh38
NC_000020.10:g.1610917C>T , CM000682.1:g.1610917C>T	GRCh37
NC_000020.9:g.1558917C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.784G>A	ENSP00000216927.4:p.Ala262Thr
ENST00000303415.7:c.1117G>A MANE Select	ENSP00000305529.3:p.Ala373Thr
ENST00000344103.8:c.466G>A	ENSP00000342759.4:p.Ala156Thr
ENST00000381580.5:c.1018G>A	ENSP00000370992.1:p.Ala340Thr
ENST00000381583.6:c.784G>A	ENSP00000370995.2:p.Ala262Thr
ENST00000478145.6:n.178G>A
ENST00000497407.2:n.266G>A
NM_001039508.1:c.784G>A	NP_001034597.1:p.Ala262Thr
NM_018556.3:c.1117G>A	NP_061026.2:p.Ala373Thr
NM_080816.2:c.466G>A	NP_543006.2:p.Ala156Thr
XM_005260749.2:c.799G>A	XP_005260806.1:p.Ala267Thr
XM_011529286.1:c.1018G>A	XP_011527588.1:p.Ala340Thr
XM_005260749.4:c.799G>A	XP_005260806.1:p.Ala267Thr
XM_011529286.2:c.1018G>A	XP_011527588.1:p.Ala340Thr
NM_018556.4:c.1117G>A MANE Select	NP_061026.2:p.Ala373Thr
NM_080816.3:c.466G>A	NP_543006.2:p.Ala156Thr
NM_001039508.2:c.784G>A	NP_001034597.1:p.Ala262Thr