Canonical Allele Identifier: CA2613258208
Gene: SLC35C1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45806097_45806098dup , CM000673.2:g.45806097_45806098dup GRCh38
NC_000011.9:g.45827648_45827649dup , CM000673.1:g.45827648_45827649dup GRCh37
NC_000011.8:g.45784224_45784225dup NCBI36
NG_009875.1:g.7026_7027dup , LRG_107:g.7026_7027dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.257_258dup ENSP00000432145.2:p.Gly87LeufsTer29
ENST00000314134.4:c.296_297dup MANE Select ENSP00000313318.3:p.Gly100LeufsTer29
ENST00000314134.3:c.296_297dup ENSP00000313318.3:p.Gly100LeufsTer29
ENST00000442528.2:c.257_258dup ENSP00000412408.2:p.Gly87LeufsTer29
ENST00000530471.1:c.257_258dup ENSP00000432669.1:p.Gly87LeufsTer29
NM_001145265.1:c.257_258dup NP_001138737.1:p.Gly87LeufsTer29
NM_001145266.1:c.257_258dup NP_001138738.1:p.Gly87LeufsTer29
NM_018389.4:c.296_297dup , LRG_107t1:c.296_297dup NP_060859.4:p.Gly100LeufsTer29
XM_011520203.1:c.296_297dup XP_011518505.1:p.Gly100LeufsTer29
XM_011520203.3:c.296_297dup XP_011518505.1:p.Gly100LeufsTer29
NM_001145265.2:c.257_258dup NP_001138737.1:p.Gly87LeufsTer29
NM_018389.5:c.296_297dup MANE Select NP_060859.4:p.Gly100LeufsTer29