Canonical Allele Identifier: CA509367588

Gene: SIRPG

Linked Data

• gnomAD v4: 20-1630266-G-A
• MyVariant Identifiers: chr20:g.1610912G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.1630266G>A , CM000682.2:g.1630266G>A	GRCh38
NC_000020.10:g.1610912G>A , CM000682.1:g.1610912G>A	GRCh37
NC_000020.9:g.1558912G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216927.4:c.789C>T	ENSP00000216927.4:p.Val263=
ENST00000303415.7:c.1122C>T MANE Select	ENSP00000305529.3:p.Val374=
ENST00000344103.8:c.471C>T	ENSP00000342759.4:p.Val157=
ENST00000381580.5:c.1023C>T	ENSP00000370992.1:p.Val341=
ENST00000381583.6:c.789C>T	ENSP00000370995.2:p.Val263=
ENST00000478145.6:n.183C>T
ENST00000497407.2:n.271C>T
NM_001039508.1:c.789C>T	NP_001034597.1:p.Val263=
NM_018556.3:c.1122C>T	NP_061026.2:p.Val374=
NM_080816.2:c.471C>T	NP_543006.2:p.Val157=
XM_005260749.2:c.804C>T	XP_005260806.1:p.Val268=
XM_011529286.1:c.1023C>T	XP_011527588.1:p.Val341=
XM_005260749.4:c.804C>T	XP_005260806.1:p.Val268=
XM_011529286.2:c.1023C>T	XP_011527588.1:p.Val341=
NM_018556.4:c.1122C>T MANE Select	NP_061026.2:p.Val374=
NM_080816.3:c.471C>T	NP_543006.2:p.Val157=
NM_001039508.2:c.789C>T	NP_001034597.1:p.Val263=