Canonical Allele Identifier: CA407998555

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610944A>C (hg19) ; chr20:g.1630298A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630298A>C , CM000682.2:g.1630298A>C	GRCh38
NC_000020.10:g.1610944A>C , CM000682.1:g.1610944A>C	GRCh37
NC_000020.9:g.1558944A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.757T>G	ENSP00000216927.4:p.Ser253Ala
ENST00000303415.7:c.1090T>G MANE Select	ENSP00000305529.3:p.Ser364Ala
ENST00000344103.8:c.439T>G	ENSP00000342759.4:p.Ser147Ala
ENST00000381580.5:c.991T>G	ENSP00000370992.1:p.Ser331Ala
ENST00000381583.6:c.757T>G	ENSP00000370995.2:p.Ser253Ala
ENST00000478145.6:n.151T>G
ENST00000497407.2:n.239T>G
NM_001039508.1:c.757T>G	NP_001034597.1:p.Ser253Ala
NM_018556.3:c.1090T>G	NP_061026.2:p.Ser364Ala
NM_080816.2:c.439T>G	NP_543006.2:p.Ser147Ala
XM_005260749.2:c.772T>G	XP_005260806.1:p.Ser258Ala
XM_011529286.1:c.991T>G	XP_011527588.1:p.Ser331Ala
XM_005260749.4:c.772T>G	XP_005260806.1:p.Ser258Ala
XM_011529286.2:c.991T>G	XP_011527588.1:p.Ser331Ala
NM_018556.4:c.1090T>G MANE Select	NP_061026.2:p.Ser364Ala
NM_080816.3:c.439T>G	NP_543006.2:p.Ser147Ala
NM_001039508.2:c.757T>G	NP_001034597.1:p.Ser253Ala