Canonical Allele Identifier: CA407998563

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610950G>C (hg19) ; chr20:g.1630304G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000216927.4:c.751C>G	ENSP00000216927.4:p.Pro251Ala
ENST00000303415.7:c.1084C>G MANE Select	ENSP00000305529.3:p.Pro362Ala
ENST00000344103.8:c.433C>G	ENSP00000342759.4:p.Pro145Ala
ENST00000381580.5:c.985C>G	ENSP00000370992.1:p.Pro329Ala
ENST00000381583.6:c.751C>G	ENSP00000370995.2:p.Pro251Ala
ENST00000478145.6:n.145C>G
ENST00000497407.2:n.233C>G
NM_001039508.1:c.751C>G	NP_001034597.1:p.Pro251Ala
NM_018556.3:c.1084C>G	NP_061026.2:p.Pro362Ala
NM_080816.2:c.433C>G	NP_543006.2:p.Pro145Ala
XM_005260749.2:c.766C>G	XP_005260806.1:p.Pro256Ala
XM_011529286.1:c.985C>G	XP_011527588.1:p.Pro329Ala
XM_005260749.4:c.766C>G	XP_005260806.1:p.Pro256Ala
XM_011529286.2:c.985C>G	XP_011527588.1:p.Pro329Ala
NM_018556.4:c.1084C>G MANE Select	NP_061026.2:p.Pro362Ala
NM_080816.3:c.433C>G	NP_543006.2:p.Pro145Ala
NM_001039508.2:c.751C>G	NP_001034597.1:p.Pro251Ala