Canonical Allele Identifier: CA9729318

Gene: SIRPG

Linked Data

• ClinVar Variation Id: 2470496
• ClinVar RCV Id: RCV003192492
• dbSNP Id: rs747232069
• ExAC: 20:1610950 G / A
• gnomAD v2: 20-1610950-G-A
• gnomAD v3: 20-1630304-G-A
• gnomAD v4: 20-1630304-G-A
• MyVariant Identifiers: chr20:g.1610950G>A (hg19) ; chr20:g.1630304G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630304G>A , CM000682.2:g.1630304G>A	GRCh38
NC_000020.10:g.1610950G>A , CM000682.1:g.1610950G>A	GRCh37
NC_000020.9:g.1558950G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.751C>T	ENSP00000216927.4:p.Pro251Ser
ENST00000303415.7:c.1084C>T MANE Select	ENSP00000305529.3:p.Pro362Ser
ENST00000344103.8:c.433C>T	ENSP00000342759.4:p.Pro145Ser
ENST00000381580.5:c.985C>T	ENSP00000370992.1:p.Pro329Ser
ENST00000381583.6:c.751C>T	ENSP00000370995.2:p.Pro251Ser
ENST00000478145.6:n.145C>T
ENST00000497407.2:n.233C>T
NM_001039508.1:c.751C>T	NP_001034597.1:p.Pro251Ser
NM_018556.3:c.1084C>T	NP_061026.2:p.Pro362Ser
NM_080816.2:c.433C>T	NP_543006.2:p.Pro145Ser
XM_005260749.2:c.766C>T	XP_005260806.1:p.Pro256Ser
XM_011529286.1:c.985C>T	XP_011527588.1:p.Pro329Ser
XM_005260749.4:c.766C>T	XP_005260806.1:p.Pro256Ser
XM_011529286.2:c.985C>T	XP_011527588.1:p.Pro329Ser
NM_018556.4:c.1084C>T MANE Select	NP_061026.2:p.Pro362Ser
NM_080816.3:c.433C>T	NP_543006.2:p.Pro145Ser
NM_001039508.2:c.751C>T	NP_001034597.1:p.Pro251Ser