Canonical Allele Identifier: CA509367573

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630245-G-T
• MyVariant Identifiers: chr20:g.1610891G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630245G>T , CM000682.2:g.1630245G>T	GRCh38
NC_000020.10:g.1610891G>T , CM000682.1:g.1610891G>T	GRCh37
NC_000020.9:g.1558891G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.810C>A	ENSP00000216927.4:p.Val270=
ENST00000303415.7:c.1143C>A MANE Select	ENSP00000305529.3:p.Val381=
ENST00000344103.8:c.492C>A	ENSP00000342759.4:p.Val164=
ENST00000381580.5:c.1044C>A	ENSP00000370992.1:p.Val348=
ENST00000381583.6:c.810C>A	ENSP00000370995.2:p.Val270=
ENST00000478145.6:n.204C>A
ENST00000497407.2:n.292C>A
NM_001039508.1:c.810C>A	NP_001034597.1:p.Val270=
NM_018556.3:c.1143C>A	NP_061026.2:p.Val381=
NM_080816.2:c.492C>A	NP_543006.2:p.Val164=
XM_005260749.2:c.825C>A	XP_005260806.1:p.Val275=
XM_011529286.1:c.1044C>A	XP_011527588.1:p.Val348=
XM_005260749.4:c.825C>A	XP_005260806.1:p.Val275=
XM_011529286.2:c.1044C>A	XP_011527588.1:p.Val348=
NM_018556.4:c.1143C>A MANE Select	NP_061026.2:p.Val381=
NM_080816.3:c.492C>A	NP_543006.2:p.Val164=
NM_001039508.2:c.810C>A	NP_001034597.1:p.Val270=