Canonical Allele Identifier: CA407998507

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610920T>A (hg19) ; chr20:g.1630274T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630274T>A , CM000682.2:g.1630274T>A	GRCh38
NC_000020.10:g.1610920T>A , CM000682.1:g.1610920T>A	GRCh37
NC_000020.9:g.1558920T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.781A>T	ENSP00000216927.4:p.Ile261Leu
ENST00000303415.7:c.1114A>T MANE Select	ENSP00000305529.3:p.Ile372Leu
ENST00000344103.8:c.463A>T	ENSP00000342759.4:p.Ile155Leu
ENST00000381580.5:c.1015A>T	ENSP00000370992.1:p.Ile339Leu
ENST00000381583.6:c.781A>T	ENSP00000370995.2:p.Ile261Leu
ENST00000478145.6:n.175A>T
ENST00000497407.2:n.263A>T
NM_001039508.1:c.781A>T	NP_001034597.1:p.Ile261Leu
NM_018556.3:c.1114A>T	NP_061026.2:p.Ile372Leu
NM_080816.2:c.463A>T	NP_543006.2:p.Ile155Leu
XM_005260749.2:c.796A>T	XP_005260806.1:p.Ile266Leu
XM_011529286.1:c.1015A>T	XP_011527588.1:p.Ile339Leu
XM_005260749.4:c.796A>T	XP_005260806.1:p.Ile266Leu
XM_011529286.2:c.1015A>T	XP_011527588.1:p.Ile339Leu
NM_018556.4:c.1114A>T MANE Select	NP_061026.2:p.Ile372Leu
NM_080816.3:c.463A>T	NP_543006.2:p.Ile155Leu
NM_001039508.2:c.781A>T	NP_001034597.1:p.Ile261Leu