Canonical Allele Identifier: CA407998463

Gene: SIRPG

Linked Data

• MyVariant Identifiers: chr20:g.1610897G>C (hg19) ; chr20:g.1630251G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630251G>C , CM000682.2:g.1630251G>C	GRCh38
NC_000020.10:g.1610897G>C , CM000682.1:g.1610897G>C	GRCh37
NC_000020.9:g.1558897G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.804C>G	ENSP00000216927.4:p.Ile268Met
ENST00000303415.7:c.1137C>G MANE Select	ENSP00000305529.3:p.Ile379Met
ENST00000344103.8:c.486C>G	ENSP00000342759.4:p.Ile162Met
ENST00000381580.5:c.1038C>G	ENSP00000370992.1:p.Ile346Met
ENST00000381583.6:c.804C>G	ENSP00000370995.2:p.Ile268Met
ENST00000478145.6:n.198C>G
ENST00000497407.2:n.286C>G
NM_001039508.1:c.804C>G	NP_001034597.1:p.Ile268Met
NM_018556.3:c.1137C>G	NP_061026.2:p.Ile379Met
NM_080816.2:c.486C>G	NP_543006.2:p.Ile162Met
XM_005260749.2:c.819C>G	XP_005260806.1:p.Ile273Met
XM_011529286.1:c.1038C>G	XP_011527588.1:p.Ile346Met
XM_005260749.4:c.819C>G	XP_005260806.1:p.Ile273Met
XM_011529286.2:c.1038C>G	XP_011527588.1:p.Ile346Met
NM_018556.4:c.1137C>G MANE Select	NP_061026.2:p.Ile379Met
NM_080816.3:c.486C>G	NP_543006.2:p.Ile162Met
NM_001039508.2:c.804C>G	NP_001034597.1:p.Ile268Met