Canonical Allele Identifier: CA2613258262

Gene: SLC35C1

Linked Data

• gnomAD v4: 11-45806400-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806400C>A , CM000673.2:g.45806400C>A	GRCh38
NC_000011.9:g.45827951C>A , CM000673.1:g.45827951C>A	GRCh37
NC_000011.8:g.45784527C>A	NCBI36
NG_009875.1:g.7329C>A , LRG_107:g.7329C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.496+64C>A	ENSP00000432145.2:n.496+64C>A
ENST00000314134.4:c.535+64C>A MANE Select	ENSP00000313318.3:n.535+64C>A
ENST00000314134.3:c.535+64C>A	ENSP00000313318.3:n.535+64C>A
ENST00000442528.2:c.496+64C>A	ENSP00000412408.2:n.496+64C>A
NM_001145265.1:c.496+64C>A	NP_001138737.1:n.496+64C>A
NM_001145266.1:c.496+64C>A	NP_001138738.1:n.496+64C>A
NM_018389.4:c.535+64C>A , LRG_107t1:c.535+64C>A	NP_060859.4:n.535+64C>A
XM_011520203.1:c.535+64C>A	XP_011518505.1:n.535+64C>A
XM_011520203.3:c.535+64C>A	XP_011518505.1:n.535+64C>A
NM_001145265.2:c.496+64C>A	NP_001138737.1:n.496+64C>A
NM_018389.5:c.535+64C>A MANE Select	NP_060859.4:n.535+64C>A