Canonical Allele Identifier: CA407998499

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630270-G-T
• MyVariant Identifiers: chr20:g.1610916G>T (hg19) ; chr20:g.1630270G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630270G>T , CM000682.2:g.1630270G>T	GRCh38
NC_000020.10:g.1610916G>T , CM000682.1:g.1610916G>T	GRCh37
NC_000020.9:g.1558916G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.785C>A	ENSP00000216927.4:p.Ala262Asp
ENST00000303415.7:c.1118C>A MANE Select	ENSP00000305529.3:p.Ala373Asp
ENST00000344103.8:c.467C>A	ENSP00000342759.4:p.Ala156Asp
ENST00000381580.5:c.1019C>A	ENSP00000370992.1:p.Ala340Asp
ENST00000381583.6:c.785C>A	ENSP00000370995.2:p.Ala262Asp
ENST00000478145.6:n.179C>A
ENST00000497407.2:n.267C>A
NM_001039508.1:c.785C>A	NP_001034597.1:p.Ala262Asp
NM_018556.3:c.1118C>A	NP_061026.2:p.Ala373Asp
NM_080816.2:c.467C>A	NP_543006.2:p.Ala156Asp
XM_005260749.2:c.800C>A	XP_005260806.1:p.Ala267Asp
XM_011529286.1:c.1019C>A	XP_011527588.1:p.Ala340Asp
XM_005260749.4:c.800C>A	XP_005260806.1:p.Ala267Asp
XM_011529286.2:c.1019C>A	XP_011527588.1:p.Ala340Asp
NM_018556.4:c.1118C>A MANE Select	NP_061026.2:p.Ala373Asp
NM_080816.3:c.467C>A	NP_543006.2:p.Ala156Asp
NM_001039508.2:c.785C>A	NP_001034597.1:p.Ala262Asp