Canonical Allele Identifier: CA2345350199
Gene: SLC52A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.765571G= , CM000682.2:g.765571G= GRCh38
NC_000020.10:g.746215G= , CM000682.1:g.746215G= GRCh37
NC_000020.9:g.694215G= NCBI36
NG_027687.1:g.8014C=
NG_027687.2:g.15415C=

Transcript Alleles

HGVS Amino-acid change
ENST00000381944.5:c.204C= ENSP00000371370.3:p.Cys68=
ENST00000473664.2:c.204C= ENSP00000502741.1:p.Cys68=
ENST00000488495.3:c.204C= ENSP00000494009.1:p.Cys68=
ENST00000645534.1:c.204C= MANE Select ENSP00000494193.1:p.Cys68=
ENST00000675066.1:c.204C= ENSP00000501902.1:p.Cys68=
ENST00000676154.1:c.204C= ENSP00000501807.1:p.Cys68=
ENST00000217254.11:c.204C= ENSP00000217254.7:p.Cys68=
ENST00000381944.4:c.204C= ENSP00000371370.3:p.Cys68=
ENST00000473664.1:n.255C=
ENST00000632431.1:c.204C= ENSP00000488723.1:p.Cys68=
NM_033409.3:c.204C= NP_212134.3:p.Cys68=
XM_005260655.3:c.204C= XP_005260712.1:p.Cys68=
XM_011529148.1:c.204C= XP_011527450.1:p.Cys68=
XM_005260655.4:c.204C= XP_005260712.1:p.Cys68=
XM_024451821.1:c.204C= XP_024307589.1:p.Cys68=
NM_033409.4:c.204C= MANE Select NP_212134.3:p.Cys68=
NM_001370085.1:c.204C= NP_001357014.1:p.Cys68=
NM_001370086.1:c.204C= NP_001357015.1:p.Cys68=