Canonical Allele Identifier: CA407998405

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630224-T-A
• MyVariant Identifiers: chr20:g.1610870T>A (hg19) ; chr20:g.1630224T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630224T>A , CM000682.2:g.1630224T>A	GRCh38
NC_000020.10:g.1610870T>A , CM000682.1:g.1610870T>A	GRCh37
NC_000020.9:g.1558870T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.831A>T	ENSP00000216927.4:p.Ter277Cys
ENST00000303415.7:c.1164A>T MANE Select	ENSP00000305529.3:p.Ter388Cys
ENST00000344103.8:c.513A>T	ENSP00000342759.4:p.Ter171Cys
ENST00000381580.5:c.1065A>T	ENSP00000370992.1:p.Ter355Cys
ENST00000381583.6:c.831A>T	ENSP00000370995.2:p.Ter277Cys
ENST00000478145.6:n.225A>T
ENST00000497407.2:n.313A>T
NM_001039508.1:c.831A>T	NP_001034597.1:p.Ter277Cys
NM_018556.3:c.1164A>T	NP_061026.2:p.Ter388Cys
NM_080816.2:c.513A>T	NP_543006.2:p.Ter171Cys
XM_005260749.2:c.846A>T	XP_005260806.1:p.Ter282Cys
XM_011529286.1:c.1065A>T	XP_011527588.1:p.Ter355Cys
XM_005260749.4:c.846A>T	XP_005260806.1:p.Ter282Cys
XM_011529286.2:c.1065A>T	XP_011527588.1:p.Ter355Cys
NM_018556.4:c.1164A>T MANE Select	NP_061026.2:p.Ter388Cys
NM_080816.3:c.513A>T	NP_543006.2:p.Ter171Cys
NM_001039508.2:c.831A>T	NP_001034597.1:p.Ter277Cys