Canonical Allele Identifier: CA407998482

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610907A>T (hg19) ; chr20:g.1630261A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630261A>T , CM000682.2:g.1630261A>T	GRCh38
NC_000020.10:g.1610907A>T , CM000682.1:g.1610907A>T	GRCh37
NC_000020.9:g.1558907A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.794T>A	ENSP00000216927.4:p.Leu265Gln
ENST00000303415.7:c.1127T>A MANE Select	ENSP00000305529.3:p.Leu376Gln
ENST00000344103.8:c.476T>A	ENSP00000342759.4:p.Leu159Gln
ENST00000381580.5:c.1028T>A	ENSP00000370992.1:p.Leu343Gln
ENST00000381583.6:c.794T>A	ENSP00000370995.2:p.Leu265Gln
ENST00000478145.6:n.188T>A
ENST00000497407.2:n.276T>A
NM_001039508.1:c.794T>A	NP_001034597.1:p.Leu265Gln
NM_018556.3:c.1127T>A	NP_061026.2:p.Leu376Gln
NM_080816.2:c.476T>A	NP_543006.2:p.Leu159Gln
XM_005260749.2:c.809T>A	XP_005260806.1:p.Leu270Gln
XM_011529286.1:c.1028T>A	XP_011527588.1:p.Leu343Gln
XM_005260749.4:c.809T>A	XP_005260806.1:p.Leu270Gln
XM_011529286.2:c.1028T>A	XP_011527588.1:p.Leu343Gln
NM_018556.4:c.1127T>A MANE Select	NP_061026.2:p.Leu376Gln
NM_080816.3:c.476T>A	NP_543006.2:p.Leu159Gln
NM_001039508.2:c.794T>A	NP_001034597.1:p.Leu265Gln