Canonical Allele Identifier: CA1968692241

Gene: SLC35C1

Linked Data

• dbSNP Id: rs1590742642
• gnomAD v4: 11-45805762-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805762C>G , CM000673.2:g.45805762C>G	GRCh38
NC_000011.9:g.45827313C>G , CM000673.1:g.45827313C>G	GRCh37
NC_000011.8:g.45783889C>G	NCBI36
NG_009875.1:g.6691C>G , LRG_107:g.6691C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.-31-48C>G	ENSP00000432145.2:n.-31-48C>G
ENST00000314134.4:c.-40C>G MANE Select	ENSP00000313318.3:n.-40C>G
ENST00000314134.3:c.-40C>G	ENSP00000313318.3:n.-40C>G
ENST00000442528.2:c.-31-48C>G	ENSP00000412408.2:n.-31-48C>G
ENST00000526817.1:c.-31-48C>G	ENSP00000432145.1:n.-31-48C>G
ENST00000530471.1:c.-31-48C>G	ENSP00000432669.1:n.-31-48C>G
NM_001145265.1:c.-31-48C>G	NP_001138737.1:n.-31-48C>G
NM_001145266.1:c.-31-48C>G	NP_001138738.1:n.-31-48C>G
NM_018389.4:c.-40C>G , LRG_107t1:c.-40C>G	NP_060859.4:n.-40C>G
XM_011520203.1:c.-40C>G	XP_011518505.1:n.-40C>G
XM_011520203.3:c.-40C>G	XP_011518505.1:n.-40C>G
NM_001145265.2:c.-31-48C>G	NP_001138737.1:n.-31-48C>G
NM_018389.5:c.-40C>G MANE Select	NP_060859.4:n.-40C>G