Canonical Allele Identifier: CA407998469

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630253-T-A
• MyVariant Identifiers: chr20:g.1610899T>A (hg19) ; chr20:g.1630253T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630253T>A , CM000682.2:g.1630253T>A	GRCh38
NC_000020.10:g.1610899T>A , CM000682.1:g.1610899T>A	GRCh37
NC_000020.9:g.1558899T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.802A>T	ENSP00000216927.4:p.Ile268Phe
ENST00000303415.7:c.1135A>T MANE Select	ENSP00000305529.3:p.Ile379Phe
ENST00000344103.8:c.484A>T	ENSP00000342759.4:p.Ile162Phe
ENST00000381580.5:c.1036A>T	ENSP00000370992.1:p.Ile346Phe
ENST00000381583.6:c.802A>T	ENSP00000370995.2:p.Ile268Phe
ENST00000478145.6:n.196A>T
ENST00000497407.2:n.284A>T
NM_001039508.1:c.802A>T	NP_001034597.1:p.Ile268Phe
NM_018556.3:c.1135A>T	NP_061026.2:p.Ile379Phe
NM_080816.2:c.484A>T	NP_543006.2:p.Ile162Phe
XM_005260749.2:c.817A>T	XP_005260806.1:p.Ile273Phe
XM_011529286.1:c.1036A>T	XP_011527588.1:p.Ile346Phe
XM_005260749.4:c.817A>T	XP_005260806.1:p.Ile273Phe
XM_011529286.2:c.1036A>T	XP_011527588.1:p.Ile346Phe
NM_018556.4:c.1135A>T MANE Select	NP_061026.2:p.Ile379Phe
NM_080816.3:c.484A>T	NP_543006.2:p.Ile162Phe
NM_001039508.2:c.802A>T	NP_001034597.1:p.Ile268Phe