Canonical Allele Identifier: CA407998428

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610880T>G (hg19) ; chr20:g.1630234T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630234T>G , CM000682.2:g.1630234T>G	GRCh38
NC_000020.10:g.1610880T>G , CM000682.1:g.1610880T>G	GRCh37
NC_000020.9:g.1558880T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.821A>C	ENSP00000216927.4:p.Gln274Pro
ENST00000303415.7:c.1154A>C MANE Select	ENSP00000305529.3:p.Gln385Pro
ENST00000344103.8:c.503A>C	ENSP00000342759.4:p.Gln168Pro
ENST00000381580.5:c.1055A>C	ENSP00000370992.1:p.Gln352Pro
ENST00000381583.6:c.821A>C	ENSP00000370995.2:p.Gln274Pro
ENST00000478145.6:n.215A>C
ENST00000497407.2:n.303A>C
NM_001039508.1:c.821A>C	NP_001034597.1:p.Gln274Pro
NM_018556.3:c.1154A>C	NP_061026.2:p.Gln385Pro
NM_080816.2:c.503A>C	NP_543006.2:p.Gln168Pro
XM_005260749.2:c.836A>C	XP_005260806.1:p.Gln279Pro
XM_011529286.1:c.1055A>C	XP_011527588.1:p.Gln352Pro
XM_005260749.4:c.836A>C	XP_005260806.1:p.Gln279Pro
XM_011529286.2:c.1055A>C	XP_011527588.1:p.Gln352Pro
NM_018556.4:c.1154A>C MANE Select	NP_061026.2:p.Gln385Pro
NM_080816.3:c.503A>C	NP_543006.2:p.Gln168Pro
NM_001039508.2:c.821A>C	NP_001034597.1:p.Gln274Pro