Canonical Allele Identifier: CA310790931

Gene: SIRPG

Linked Data

• dbSNP Id: rs896783369
• MyVariant Identifiers: chr20:g.1610597C>T (hg19) ; chr20:g.1629951C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1629951C>T , CM000682.2:g.1629951C>T	GRCh38
NC_000020.10:g.1610597C>T , CM000682.1:g.1610597C>T	GRCh37
NC_000020.9:g.1558597C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303415.7:c.*2+271G>A MANE Select	ENSP00000305529.3:n.*2+271G>A
ENST00000344103.8:c.*2+271G>A	ENSP00000342759.4:n.*2+271G>A
ENST00000381580.5:c.*2+271G>A	ENSP00000370992.1:n.*2+271G>A
ENST00000381583.6:c.*2+271G>A	ENSP00000370995.2:n.*2+271G>A
ENST00000478145.6:n.227+271G>A
ENST00000497407.2:n.315+271G>A
NM_001039508.1:c.*2+271G>A	NP_001034597.1:n.*2+271G>A
NM_018556.3:c.*2+271G>A	NP_061026.2:n.*2+271G>A
NM_080816.2:c.*2+271G>A	NP_543006.2:n.*2+271G>A
XM_005260749.2:c.*2+271G>A	XP_005260806.1:n.*2+271G>A
XM_011529286.1:c.*2+271G>A	XP_011527588.1:n.*2+271G>A
XM_005260749.4:c.*2+271G>A	XP_005260806.1:n.*2+271G>A
XM_011529286.2:c.*2+271G>A	XP_011527588.1:n.*2+271G>A
NM_018556.4:c.*2+271G>A MANE Select	NP_061026.2:n.*2+271G>A
NM_080816.3:c.*2+271G>A	NP_543006.2:n.*2+271G>A
NM_001039508.2:c.*2+271G>A	NP_001034597.1:n.*2+271G>A