Canonical Allele Identifier: CA340708543
Gene: SLC35D1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053875C>G , CM000663.2:g.67053875C>G GRCh38
NC_000001.10:g.67519558C>G , CM000663.1:g.67519558C>G GRCh37
NC_000001.9:g.67292146C>G NCBI36
NG_012933.1:g.5523G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.139G>C MANE Select ENSP00000235345.5:p.Gly47Arg
ENST00000235345.5:c.139G>C ENSP00000235345.5:p.Gly47Arg
NM_015139.2:c.139G>C NP_055954.1:p.Gly47Arg
XM_006710478.1:c.139G>C XP_006710541.1:p.Gly47Arg
XM_011541070.1:c.139G>C XP_011539372.1:p.Gly47Arg
XM_006710478.2:c.139G>C XP_006710541.1:p.Gly47Arg
XM_011541070.2:c.139G>C XP_011539372.1:p.Gly47Arg
XR_001737057.2:n.549G>C
XR_001737058.2:n.542G>C
NM_015139.3:c.139G>C MANE Select NP_055954.1:p.Gly47Arg