Canonical Allele Identifier: CA407998414

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630229-T-C
• MyVariant Identifiers: chr20:g.1610875T>C (hg19) ; chr20:g.1630229T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630229T>C , CM000682.2:g.1630229T>C	GRCh38
NC_000020.10:g.1610875T>C , CM000682.1:g.1610875T>C	GRCh37
NC_000020.9:g.1558875T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.826A>G	ENSP00000216927.4:p.Thr276Ala
ENST00000303415.7:c.1159A>G MANE Select	ENSP00000305529.3:p.Thr387Ala
ENST00000344103.8:c.508A>G	ENSP00000342759.4:p.Thr170Ala
ENST00000381580.5:c.1060A>G	ENSP00000370992.1:p.Thr354Ala
ENST00000381583.6:c.826A>G	ENSP00000370995.2:p.Thr276Ala
ENST00000478145.6:n.220A>G
ENST00000497407.2:n.308A>G
NM_001039508.1:c.826A>G	NP_001034597.1:p.Thr276Ala
NM_018556.3:c.1159A>G	NP_061026.2:p.Thr387Ala
NM_080816.2:c.508A>G	NP_543006.2:p.Thr170Ala
XM_005260749.2:c.841A>G	XP_005260806.1:p.Thr281Ala
XM_011529286.1:c.1060A>G	XP_011527588.1:p.Thr354Ala
XM_005260749.4:c.841A>G	XP_005260806.1:p.Thr281Ala
XM_011529286.2:c.1060A>G	XP_011527588.1:p.Thr354Ala
NM_018556.4:c.1159A>G MANE Select	NP_061026.2:p.Thr387Ala
NM_080816.3:c.508A>G	NP_543006.2:p.Thr170Ala
NM_001039508.2:c.826A>G	NP_001034597.1:p.Thr276Ala