Canonical Allele Identifier: CA407998559

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610947C>G (hg19) ; chr20:g.1630301C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630301C>G , CM000682.2:g.1630301C>G	GRCh38
NC_000020.10:g.1610947C>G , CM000682.1:g.1610947C>G	GRCh37
NC_000020.9:g.1558947C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.754G>C	ENSP00000216927.4:p.Ala252Pro
ENST00000303415.7:c.1087G>C MANE Select	ENSP00000305529.3:p.Ala363Pro
ENST00000344103.8:c.436G>C	ENSP00000342759.4:p.Ala146Pro
ENST00000381580.5:c.988G>C	ENSP00000370992.1:p.Ala330Pro
ENST00000381583.6:c.754G>C	ENSP00000370995.2:p.Ala252Pro
ENST00000478145.6:n.148G>C
ENST00000497407.2:n.236G>C
NM_001039508.1:c.754G>C	NP_001034597.1:p.Ala252Pro
NM_018556.3:c.1087G>C	NP_061026.2:p.Ala363Pro
NM_080816.2:c.436G>C	NP_543006.2:p.Ala146Pro
XM_005260749.2:c.769G>C	XP_005260806.1:p.Ala257Pro
XM_011529286.1:c.988G>C	XP_011527588.1:p.Ala330Pro
XM_005260749.4:c.769G>C	XP_005260806.1:p.Ala257Pro
XM_011529286.2:c.988G>C	XP_011527588.1:p.Ala330Pro
NM_018556.4:c.1087G>C MANE Select	NP_061026.2:p.Ala363Pro
NM_080816.3:c.436G>C	NP_543006.2:p.Ala146Pro
NM_001039508.2:c.754G>C	NP_001034597.1:p.Ala252Pro