Canonical Allele Identifier: CA407998437

Gene: SIRPG

Linked Data

• dbSNP Id: rs1400827235
• gnomAD v2: 20-1610885-C-A
• gnomAD v4: 20-1630239-C-A
• MyVariant Identifiers: chr20:g.1610885C>A (hg19) ; chr20:g.1630239C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630239C>A , CM000682.2:g.1630239C>A	GRCh38
NC_000020.10:g.1610885C>A , CM000682.1:g.1610885C>A	GRCh37
NC_000020.9:g.1558885C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.816G>T	ENSP00000216927.4:p.Trp272Cys
ENST00000303415.7:c.1149G>T MANE Select	ENSP00000305529.3:p.Trp383Cys
ENST00000344103.8:c.498G>T	ENSP00000342759.4:p.Trp166Cys
ENST00000381580.5:c.1050G>T	ENSP00000370992.1:p.Trp350Cys
ENST00000381583.6:c.816G>T	ENSP00000370995.2:p.Trp272Cys
ENST00000478145.6:n.210G>T
ENST00000497407.2:n.298G>T
NM_001039508.1:c.816G>T	NP_001034597.1:p.Trp272Cys
NM_018556.3:c.1149G>T	NP_061026.2:p.Trp383Cys
NM_080816.2:c.498G>T	NP_543006.2:p.Trp166Cys
XM_005260749.2:c.831G>T	XP_005260806.1:p.Trp277Cys
XM_011529286.1:c.1050G>T	XP_011527588.1:p.Trp350Cys
XM_005260749.4:c.831G>T	XP_005260806.1:p.Trp277Cys
XM_011529286.2:c.1050G>T	XP_011527588.1:p.Trp350Cys
NM_018556.4:c.1149G>T MANE Select	NP_061026.2:p.Trp383Cys
NM_080816.3:c.498G>T	NP_543006.2:p.Trp166Cys
NM_001039508.2:c.816G>T	NP_001034597.1:p.Trp272Cys