Canonical Allele Identifier: CA407998494

Gene: SIRPG

Linked Data

• dbSNP Id: rs1286427526
• gnomAD v2: 20-1610914-C-T
• gnomAD v4: 20-1630268-C-T
• MyVariant Identifiers: chr20:g.1610914C>T (hg19) ; chr20:g.1630268C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630268C>T , CM000682.2:g.1630268C>T	GRCh38
NC_000020.10:g.1610914C>T , CM000682.1:g.1610914C>T	GRCh37
NC_000020.9:g.1558914C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.787G>A	ENSP00000216927.4:p.Val263Ile
ENST00000303415.7:c.1120G>A MANE Select	ENSP00000305529.3:p.Val374Ile
ENST00000344103.8:c.469G>A	ENSP00000342759.4:p.Val157Ile
ENST00000381580.5:c.1021G>A	ENSP00000370992.1:p.Val341Ile
ENST00000381583.6:c.787G>A	ENSP00000370995.2:p.Val263Ile
ENST00000478145.6:n.181G>A
ENST00000497407.2:n.269G>A
NM_001039508.1:c.787G>A	NP_001034597.1:p.Val263Ile
NM_018556.3:c.1120G>A	NP_061026.2:p.Val374Ile
NM_080816.2:c.469G>A	NP_543006.2:p.Val157Ile
XM_005260749.2:c.802G>A	XP_005260806.1:p.Val268Ile
XM_011529286.1:c.1021G>A	XP_011527588.1:p.Val341Ile
XM_005260749.4:c.802G>A	XP_005260806.1:p.Val268Ile
XM_011529286.2:c.1021G>A	XP_011527588.1:p.Val341Ile
NM_018556.4:c.1120G>A MANE Select	NP_061026.2:p.Val374Ile
NM_080816.3:c.469G>A	NP_543006.2:p.Val157Ile
NM_001039508.2:c.787G>A	NP_001034597.1:p.Val263Ile