Canonical Allele Identifier: CA407998552

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610943G>C (hg19) ; chr20:g.1630297G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630297G>C , CM000682.2:g.1630297G>C	GRCh38
NC_000020.10:g.1610943G>C , CM000682.1:g.1610943G>C	GRCh37
NC_000020.9:g.1558943G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.758C>G	ENSP00000216927.4:p.Ser253Ter
ENST00000303415.7:c.1091C>G MANE Select	ENSP00000305529.3:p.Ser364Ter
ENST00000344103.8:c.440C>G	ENSP00000342759.4:p.Ser147Ter
ENST00000381580.5:c.992C>G	ENSP00000370992.1:p.Ser331Ter
ENST00000381583.6:c.758C>G	ENSP00000370995.2:p.Ser253Ter
ENST00000478145.6:n.152C>G
ENST00000497407.2:n.240C>G
NM_001039508.1:c.758C>G	NP_001034597.1:p.Ser253Ter
NM_018556.3:c.1091C>G	NP_061026.2:p.Ser364Ter
NM_080816.2:c.440C>G	NP_543006.2:p.Ser147Ter
XM_005260749.2:c.773C>G	XP_005260806.1:p.Ser258Ter
XM_011529286.1:c.992C>G	XP_011527588.1:p.Ser331Ter
XM_005260749.4:c.773C>G	XP_005260806.1:p.Ser258Ter
XM_011529286.2:c.992C>G	XP_011527588.1:p.Ser331Ter
NM_018556.4:c.1091C>G MANE Select	NP_061026.2:p.Ser364Ter
NM_080816.3:c.440C>G	NP_543006.2:p.Ser147Ter
NM_001039508.2:c.758C>G	NP_001034597.1:p.Ser253Ter