Canonical Allele Identifier: CA509367618

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610948C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630302C>G , CM000682.2:g.1630302C>G	GRCh38
NC_000020.10:g.1610948C>G , CM000682.1:g.1610948C>G	GRCh37
NC_000020.9:g.1558948C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.753G>C	ENSP00000216927.4:p.Pro251=
ENST00000303415.7:c.1086G>C MANE Select	ENSP00000305529.3:p.Pro362=
ENST00000344103.8:c.435G>C	ENSP00000342759.4:p.Pro145=
ENST00000381580.5:c.987G>C	ENSP00000370992.1:p.Pro329=
ENST00000381583.6:c.753G>C	ENSP00000370995.2:p.Pro251=
ENST00000478145.6:n.147G>C
ENST00000497407.2:n.235G>C
NM_001039508.1:c.753G>C	NP_001034597.1:p.Pro251=
NM_018556.3:c.1086G>C	NP_061026.2:p.Pro362=
NM_080816.2:c.435G>C	NP_543006.2:p.Pro145=
XM_005260749.2:c.768G>C	XP_005260806.1:p.Pro256=
XM_011529286.1:c.987G>C	XP_011527588.1:p.Pro329=
XM_005260749.4:c.768G>C	XP_005260806.1:p.Pro256=
XM_011529286.2:c.987G>C	XP_011527588.1:p.Pro329=
NM_018556.4:c.1086G>C MANE Select	NP_061026.2:p.Pro362=
NM_080816.3:c.435G>C	NP_543006.2:p.Pro145=
NM_001039508.2:c.753G>C	NP_001034597.1:p.Pro251=