Canonical Allele Identifier: CA2613258240

Gene: SLC35C1

Linked Data

• gnomAD v4: 11-45806376-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806376G>T , CM000673.2:g.45806376G>T	GRCh38
NC_000011.9:g.45827927G>T , CM000673.1:g.45827927G>T	GRCh37
NC_000011.8:g.45784503G>T	NCBI36
NG_009875.1:g.7305G>T , LRG_107:g.7305G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.496+40G>T	ENSP00000432145.2:n.496+40G>T
ENST00000314134.4:c.535+40G>T MANE Select	ENSP00000313318.3:n.535+40G>T
ENST00000314134.3:c.535+40G>T	ENSP00000313318.3:n.535+40G>T
ENST00000442528.2:c.496+40G>T	ENSP00000412408.2:n.496+40G>T
NM_001145265.1:c.496+40G>T	NP_001138737.1:n.496+40G>T
NM_001145266.1:c.496+40G>T	NP_001138738.1:n.496+40G>T
NM_018389.4:c.535+40G>T , LRG_107t1:c.535+40G>T	NP_060859.4:n.535+40G>T
XM_011520203.1:c.535+40G>T	XP_011518505.1:n.535+40G>T
XM_011520203.3:c.535+40G>T	XP_011518505.1:n.535+40G>T
NM_001145265.2:c.496+40G>T	NP_001138737.1:n.496+40G>T
NM_018389.5:c.535+40G>T MANE Select	NP_060859.4:n.535+40G>T