Canonical Allele Identifier: CA380202864
Gene: SLC35C1 HGNC NCBI

Linked Data

dbSNP Id: rs1030028421

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45806186A>C , CM000673.2:g.45806186A>C GRCh38
NC_000011.9:g.45827737A>C , CM000673.1:g.45827737A>C GRCh37
NC_000011.8:g.45784313A>C NCBI36
NG_009875.1:g.7115A>C , LRG_107:g.7115A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.346A>C ENSP00000432145.2:p.Thr116Pro
ENST00000314134.4:c.385A>C MANE Select ENSP00000313318.3:p.Thr129Pro
ENST00000314134.3:c.385A>C ENSP00000313318.3:p.Thr129Pro
ENST00000442528.2:c.346A>C ENSP00000412408.2:p.Thr116Pro
ENST00000530471.1:c.346A>C ENSP00000432669.1:p.Thr116Pro
NM_001145265.1:c.346A>C NP_001138737.1:p.Thr116Pro
NM_001145266.1:c.346A>C NP_001138738.1:p.Thr116Pro
NM_018389.4:c.385A>C , LRG_107t1:c.385A>C NP_060859.4:p.Thr129Pro
XM_011520203.1:c.385A>C XP_011518505.1:p.Thr129Pro
XM_011520203.3:c.385A>C XP_011518505.1:p.Thr129Pro
NM_001145265.2:c.346A>C NP_001138737.1:p.Thr116Pro
NM_018389.5:c.385A>C MANE Select NP_060859.4:p.Thr129Pro