Canonical Allele Identifier: CA676889125

Gene: SLC35C1

Linked Data

• dbSNP Id: rs1212541376
• MyVariant Identifiers: chr11:g.45827500_45827501insAGGAT (hg19) ; chr11:g.45805949_45805950insAGGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805949_45805950insAGGAT , CM000673.2:g.45805949_45805950insAGGAT	GRCh38
NC_000011.9:g.45827500_45827501insAGGAT , CM000673.1:g.45827500_45827501insAGGAT	GRCh37
NC_000011.8:g.45784076_45784077insAGGAT	NCBI36
NG_009875.1:g.6878_6879insAGGAT , LRG_107:g.6878_6879insAGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.109_110insAGGAT	ENSP00000432145.2:p.Val37GlufsTer?
ENST00000314134.4:c.148_149insAGGAT MANE Select	ENSP00000313318.3:p.Val50GlufsTer?
ENST00000314134.3:c.148_149insAGGAT	ENSP00000313318.3:p.Val50GlufsTer?
ENST00000442528.2:c.109_110insAGGAT	ENSP00000412408.2:p.Val37GlufsTer?
ENST00000526817.1:c.109_110insAGGAT	ENSP00000432145.1:p.Val37GlufsTer?
ENST00000530471.1:c.109_110insAGGAT	ENSP00000432669.1:p.Val37GlufsTer?
NM_001145265.1:c.109_110insAGGAT	NP_001138737.1:p.Val37GlufsTer?
NM_001145266.1:c.109_110insAGGAT	NP_001138738.1:p.Val37GlufsTer?
NM_018389.4:c.148_149insAGGAT , LRG_107t1:c.148_149insAGGAT	NP_060859.4:p.Val50GlufsTer?
XM_011520203.1:c.148_149insAGGAT	XP_011518505.1:p.Val50GlufsTer?
XM_011520203.3:c.148_149insAGGAT	XP_011518505.1:p.Val50GlufsTer?
NM_001145265.2:c.109_110insAGGAT	NP_001138737.1:p.Val37GlufsTer?
NM_018389.5:c.148_149insAGGAT MANE Select	NP_060859.4:p.Val50GlufsTer?