Canonical Allele Identifier: CA412894143
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2783570
ClinVar RCV Id: RCV003741426
gnomAD v4: X-48904819-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48904819G>A , CM000685.2:g.48904819G>A GRCh38
NC_000023.10:g.48762096G>A , CM000685.1:g.48762096G>A GRCh37
NC_000023.9:g.48647040G>A NCBI36
NG_015967.1:g.11902G>A
NG_034300.1:g.12140C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000247138.11:c.1090C>T MANE Select ENSP00000247138.5:p.Pro364Ser
ENST00000247138.10:c.1090C>T ENSP00000247138.5:p.Pro364Ser
ENST00000376515.8:c.428C>T ENSP00000365698.3:p.Ala143Val
ENST00000376521.6:c.1090C>T ENSP00000365704.1:p.Pro364Ser
ENST00000376529.8:c.500C>T ENSP00000365712.3:p.Ala167Val
ENST00000413561.7:c.652C>T
ENST00000445167.7:c.500C>T ENSP00000402726.2:p.Ala167Val
ENST00000452555.7:c.1174C>T ENSP00000416002.2:p.Pro392Ser
ENST00000616181.5:c.1129C>T ENSP00000478617.1:p.Pro377Ser
ENST00000635285.1:c.1090C>T ENSP00000489484.1:p.Pro364Ser
ENST00000635460.1:c.425-1354C>T
ENST00000635589.1:c.907C>T ENSP00000489197.1:p.Pro303Ser
ENST00000635628.1:c.*984C>T ENSP00000489613.1:n.*984C>T
NM_001032289.2:c.500C>T NP_001027460.1:p.Ala167Val
NM_001042498.2:c.1090C>T NP_001035963.1:p.Pro364Ser
NM_001282647.1:c.500C>T NP_001269576.1:p.Ala167Val
NM_001282648.1:c.428C>T NP_001269577.1:p.Ala143Val
NM_001282649.1:c.907C>T NP_001269578.1:p.Pro303Ser
NM_001282650.1:c.1129C>T NP_001269579.1:p.Pro377Ser
NM_001282651.1:c.1174C>T NP_001269580.1:p.Pro392Ser
NM_005660.2:c.1090C>T NP_005651.1:p.Pro364Ser
NM_005660.3:c.1090C>T MANE Select NP_005651.1:p.Pro364Ser
NM_001032289.3:c.500C>T NP_001027460.1:p.Ala167Val
NM_001042498.3:c.1090C>T NP_001035963.1:p.Pro364Ser
NM_001282647.2:c.500C>T NP_001269576.1:p.Ala167Val
NM_001282649.2:c.907C>T NP_001269578.1:p.Pro303Ser
NM_001282650.2:c.1129C>T NP_001269579.1:p.Pro377Ser
NM_001282651.2:c.1174C>T NP_001269580.1:p.Pro392Ser
NM_001282648.2:c.428C>T NP_001269577.1:p.Ala143Val