Canonical Allele Identifier: CA221584914
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1381648
ClinVar RCV Id: RCV001922018
dbSNP Id: rs538320044

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805811G>A , CM000673.2:g.45805811G>A GRCh38
NC_000011.9:g.45827362G>A , CM000673.1:g.45827362G>A GRCh37
NC_000011.8:g.45783938G>A NCBI36
NG_009875.1:g.6740G>A , LRG_107:g.6740G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.-30G>A ENSP00000432145.2:n.-30G>A
ENST00000314134.4:c.10G>A MANE Select ENSP00000313318.3:p.Ala4Thr
ENST00000314134.3:c.10G>A ENSP00000313318.3:p.Ala4Thr
ENST00000442528.2:c.-30G>A ENSP00000412408.2:n.-30G>A
ENST00000526817.1:c.-30G>A ENSP00000432145.1:n.-30G>A
ENST00000530471.1:c.-30G>A ENSP00000432669.1:n.-30G>A
NM_001145265.1:c.-30G>A NP_001138737.1:n.-30G>A
NM_001145266.1:c.-30G>A NP_001138738.1:n.-30G>A
NM_018389.4:c.10G>A , LRG_107t1:c.10G>A NP_060859.4:p.Ala4Thr
XM_011520203.1:c.10G>A XP_011518505.1:p.Ala4Thr
XM_011520203.3:c.10G>A XP_011518505.1:p.Ala4Thr
NM_001145265.2:c.-30G>A NP_001138737.1:n.-30G>A
NM_018389.5:c.10G>A MANE Select NP_060859.4:p.Ala4Thr