Canonical Allele Identifier: CA407998535

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610935T>G (hg19) ; chr20:g.1630289T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630289T>G , CM000682.2:g.1630289T>G	GRCh38
NC_000020.10:g.1610935T>G , CM000682.1:g.1610935T>G	GRCh37
NC_000020.9:g.1558935T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.766A>C	ENSP00000216927.4:p.Thr256Pro
ENST00000303415.7:c.1099A>C MANE Select	ENSP00000305529.3:p.Thr367Pro
ENST00000344103.8:c.448A>C	ENSP00000342759.4:p.Thr150Pro
ENST00000381580.5:c.1000A>C	ENSP00000370992.1:p.Thr334Pro
ENST00000381583.6:c.766A>C	ENSP00000370995.2:p.Thr256Pro
ENST00000478145.6:n.160A>C
ENST00000497407.2:n.248A>C
NM_001039508.1:c.766A>C	NP_001034597.1:p.Thr256Pro
NM_018556.3:c.1099A>C	NP_061026.2:p.Thr367Pro
NM_080816.2:c.448A>C	NP_543006.2:p.Thr150Pro
XM_005260749.2:c.781A>C	XP_005260806.1:p.Thr261Pro
XM_011529286.1:c.1000A>C	XP_011527588.1:p.Thr334Pro
XM_005260749.4:c.781A>C	XP_005260806.1:p.Thr261Pro
XM_011529286.2:c.1000A>C	XP_011527588.1:p.Thr334Pro
NM_018556.4:c.1099A>C MANE Select	NP_061026.2:p.Thr367Pro
NM_080816.3:c.448A>C	NP_543006.2:p.Thr150Pro
NM_001039508.2:c.766A>C	NP_001034597.1:p.Thr256Pro