Canonical Allele Identifier: CA380201976
Gene: SLC35C1 HGNC NCBI

Linked Data

dbSNP Id: rs2085864872

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805832A>G , CM000673.2:g.45805832A>G GRCh38
NC_000011.9:g.45827383A>G , CM000673.1:g.45827383A>G GRCh37
NC_000011.8:g.45783959A>G NCBI36
NG_009875.1:g.6761A>G , LRG_107:g.6761A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.-9A>G ENSP00000432145.2:n.-9A>G
ENST00000314134.4:c.31A>G MANE Select ENSP00000313318.3:p.Ile11Val
ENST00000314134.3:c.31A>G ENSP00000313318.3:p.Ile11Val
ENST00000442528.2:c.-9A>G ENSP00000412408.2:n.-9A>G
ENST00000526817.1:c.-9A>G ENSP00000432145.1:n.-9A>G
ENST00000530471.1:c.-9A>G ENSP00000432669.1:n.-9A>G
NM_001145265.1:c.-9A>G NP_001138737.1:n.-9A>G
NM_001145266.1:c.-9A>G NP_001138738.1:n.-9A>G
NM_018389.4:c.31A>G , LRG_107t1:c.31A>G NP_060859.4:p.Ile11Val
XM_011520203.1:c.31A>G XP_011518505.1:p.Ile11Val
XM_011520203.3:c.31A>G XP_011518505.1:p.Ile11Val
NM_001145265.2:c.-9A>G NP_001138737.1:n.-9A>G
NM_018389.5:c.31A>G MANE Select NP_060859.4:p.Ile11Val