Canonical Allele Identifier: CA2613258200
Gene: SLC35C1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805949_45805950insAGGA , CM000673.2:g.45805949_45805950insAGGA GRCh38
NC_000011.9:g.45827500_45827501insAGGA , CM000673.1:g.45827500_45827501insAGGA GRCh37
NC_000011.8:g.45784076_45784077insAGGA NCBI36
NG_009875.1:g.6878_6879insAGGA , LRG_107:g.6878_6879insAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.109_110insAGGA ENSP00000432145.2:p.Val37GlufsTer11
ENST00000314134.4:c.148_149insAGGA MANE Select ENSP00000313318.3:p.Val50GlufsTer11
ENST00000314134.3:c.148_149insAGGA ENSP00000313318.3:p.Val50GlufsTer11
ENST00000442528.2:c.109_110insAGGA ENSP00000412408.2:p.Val37GlufsTer11
ENST00000526817.1:c.109_110insAGGA ENSP00000432145.1:p.Val37GlufsTer11
ENST00000530471.1:c.109_110insAGGA ENSP00000432669.1:p.Val37GlufsTer11
NM_001145265.1:c.109_110insAGGA NP_001138737.1:p.Val37GlufsTer11
NM_001145266.1:c.109_110insAGGA NP_001138738.1:p.Val37GlufsTer11
NM_018389.4:c.148_149insAGGA , LRG_107t1:c.148_149insAGGA NP_060859.4:p.Val50GlufsTer11
XM_011520203.1:c.148_149insAGGA XP_011518505.1:p.Val50GlufsTer11
XM_011520203.3:c.148_149insAGGA XP_011518505.1:p.Val50GlufsTer11
NM_001145265.2:c.109_110insAGGA NP_001138737.1:p.Val37GlufsTer11
NM_018389.5:c.148_149insAGGA MANE Select NP_060859.4:p.Val50GlufsTer11