Canonical Allele Identifier: CA509367574
Gene: SIRPG HGNC NCBI

Linked Data

gnomAD v4: 20-1630251-G-A
MyVariant Identifiers: chr20:g.1610897G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000216927.4:c.804C>T ENSP00000216927.4:p.Ile268=
ENST00000303415.7:c.1137C>T MANE Select ENSP00000305529.3:p.Ile379=
ENST00000344103.8:c.486C>T ENSP00000342759.4:p.Ile162=
ENST00000381580.5:c.1038C>T ENSP00000370992.1:p.Ile346=
ENST00000381583.6:c.804C>T ENSP00000370995.2:p.Ile268=
ENST00000478145.6:n.198C>T
ENST00000497407.2:n.286C>T
NM_001039508.1:c.804C>T NP_001034597.1:p.Ile268=
NM_018556.3:c.1137C>T NP_061026.2:p.Ile379=
NM_080816.2:c.486C>T NP_543006.2:p.Ile162=
XM_005260749.2:c.819C>T XP_005260806.1:p.Ile273=
XM_011529286.1:c.1038C>T XP_011527588.1:p.Ile346=
XM_005260749.4:c.819C>T XP_005260806.1:p.Ile273=
XM_011529286.2:c.1038C>T XP_011527588.1:p.Ile346=
NM_018556.4:c.1137C>T MANE Select NP_061026.2:p.Ile379=
NM_080816.3:c.486C>T NP_543006.2:p.Ile162=
NM_001039508.2:c.804C>T NP_001034597.1:p.Ile268=