Canonical Allele Identifier: CA407998503

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630272-T-C
• MyVariant Identifiers: chr20:g.1610918T>C (hg19) ; chr20:g.1630272T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630272T>C , CM000682.2:g.1630272T>C	GRCh38
NC_000020.10:g.1610918T>C , CM000682.1:g.1610918T>C	GRCh37
NC_000020.9:g.1558918T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.783A>G	ENSP00000216927.4:p.Ile261Met
ENST00000303415.7:c.1116A>G MANE Select	ENSP00000305529.3:p.Ile372Met
ENST00000344103.8:c.465A>G	ENSP00000342759.4:p.Ile155Met
ENST00000381580.5:c.1017A>G	ENSP00000370992.1:p.Ile339Met
ENST00000381583.6:c.783A>G	ENSP00000370995.2:p.Ile261Met
ENST00000478145.6:n.177A>G
ENST00000497407.2:n.265A>G
NM_001039508.1:c.783A>G	NP_001034597.1:p.Ile261Met
NM_018556.3:c.1116A>G	NP_061026.2:p.Ile372Met
NM_080816.2:c.465A>G	NP_543006.2:p.Ile155Met
XM_005260749.2:c.798A>G	XP_005260806.1:p.Ile266Met
XM_011529286.1:c.1017A>G	XP_011527588.1:p.Ile339Met
XM_005260749.4:c.798A>G	XP_005260806.1:p.Ile266Met
XM_011529286.2:c.1017A>G	XP_011527588.1:p.Ile339Met
NM_018556.4:c.1116A>G MANE Select	NP_061026.2:p.Ile372Met
NM_080816.3:c.465A>G	NP_543006.2:p.Ile155Met
NM_001039508.2:c.783A>G	NP_001034597.1:p.Ile261Met