Canonical Allele Identifier: CA741594621

Gene: SIRPG

Linked Data

• dbSNP Id: rs2281808
• MyVariant Identifiers: chr20:g.1610551T>A (hg19) ; chr20:g.1629905T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629905T>A , CM000682.2:g.1629905T>A	GRCh38
NC_000020.10:g.1610551T>A , CM000682.1:g.1610551T>A	GRCh37
NC_000020.9:g.1558551T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000303415.7:c.*3-269A>T MANE Select	ENSP00000305529.3:n.*3-269A>T
ENST00000344103.8:c.*3-269A>T	ENSP00000342759.4:n.*3-269A>T
ENST00000381580.5:c.*3-269A>T	ENSP00000370992.1:n.*3-269A>T
ENST00000381583.6:c.*3-269A>T	ENSP00000370995.2:n.*3-269A>T
ENST00000478145.6:n.228-269A>T
ENST00000497407.2:n.316-269A>T
NM_001039508.1:c.*3-269A>T	NP_001034597.1:n.*3-269A>T
NM_018556.3:c.*3-269A>T	NP_061026.2:n.*3-269A>T
NM_080816.2:c.*3-269A>T	NP_543006.2:n.*3-269A>T
XM_005260749.2:c.*3-269A>T	XP_005260806.1:n.*3-269A>T
XM_011529286.1:c.*3-269A>T	XP_011527588.1:n.*3-269A>T
XM_005260749.4:c.*3-269A>T	XP_005260806.1:n.*3-269A>T
XM_011529286.2:c.*3-269A>T	XP_011527588.1:n.*3-269A>T
NM_018556.4:c.*3-269A>T MANE Select	NP_061026.2:n.*3-269A>T
NM_080816.3:c.*3-269A>T	NP_543006.2:n.*3-269A>T
NM_001039508.2:c.*3-269A>T	NP_001034597.1:n.*3-269A>T