Canonical Allele Identifier: CA2842786560
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45806341G>A , CM000673.2:g.45806341G>A GRCh38
NC_000011.9:g.45827892G>A , CM000673.1:g.45827892G>A GRCh37
NC_000011.8:g.45784468G>A NCBI36
NG_009875.1:g.7270G>A , LRG_107:g.7270G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.496+5G>A ENSP00000432145.2:n.496+5G>A
ENST00000314134.4:c.535+5G>A MANE Select ENSP00000313318.3:n.535+5G>A
ENST00000314134.3:c.535+5G>A ENSP00000313318.3:n.535+5G>A
ENST00000442528.2:c.496+5G>A ENSP00000412408.2:n.496+5G>A
NM_001145265.1:c.496+5G>A NP_001138737.1:n.496+5G>A
NM_001145266.1:c.496+5G>A NP_001138738.1:n.496+5G>A
NM_018389.4:c.535+5G>A , LRG_107t1:c.535+5G>A NP_060859.4:n.535+5G>A
XM_011520203.1:c.535+5G>A XP_011518505.1:n.535+5G>A
XM_011520203.3:c.535+5G>A XP_011518505.1:n.535+5G>A
NM_001145265.2:c.496+5G>A NP_001138737.1:n.496+5G>A
NM_018389.5:c.535+5G>A MANE Select NP_060859.4:n.535+5G>A