Canonical Allele Identifier: CA9729315

Gene: SIRPG

Linked Data

• dbSNP Id: rs748516544
• ExAC: 20:1610947 C / A
• gnomAD v4: 20-1630301-C-A
• MyVariant Identifiers: chr20:g.1610947C>A (hg19) ; chr20:g.1630301C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.754G>T	ENSP00000216927.4:p.Ala252Ser
ENST00000303415.7:c.1087G>T MANE Select	ENSP00000305529.3:p.Ala363Ser
ENST00000344103.8:c.436G>T	ENSP00000342759.4:p.Ala146Ser
ENST00000381580.5:c.988G>T	ENSP00000370992.1:p.Ala330Ser
ENST00000381583.6:c.754G>T	ENSP00000370995.2:p.Ala252Ser
ENST00000478145.6:n.148G>T
ENST00000497407.2:n.236G>T
NM_001039508.1:c.754G>T	NP_001034597.1:p.Ala252Ser
NM_018556.3:c.1087G>T	NP_061026.2:p.Ala363Ser
NM_080816.2:c.436G>T	NP_543006.2:p.Ala146Ser
XM_005260749.2:c.769G>T	XP_005260806.1:p.Ala257Ser
XM_011529286.1:c.988G>T	XP_011527588.1:p.Ala330Ser
XM_005260749.4:c.769G>T	XP_005260806.1:p.Ala257Ser
XM_011529286.2:c.988G>T	XP_011527588.1:p.Ala330Ser
NM_018556.4:c.1087G>T MANE Select	NP_061026.2:p.Ala363Ser
NM_080816.3:c.436G>T	NP_543006.2:p.Ala146Ser
NM_001039508.2:c.754G>T	NP_001034597.1:p.Ala252Ser