Canonical Allele Identifier: CA1968693130
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45806353G= , CM000673.2:g.45806353G= GRCh38
NC_000011.9:g.45827904G= , CM000673.1:g.45827904G= GRCh37
NC_000011.8:g.45784480G= NCBI36
NG_009875.1:g.7282G= , LRG_107:g.7282G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.496+17G= ENSP00000432145.2:n.496+17G=
ENST00000314134.4:c.535+17G= MANE Select ENSP00000313318.3:n.535+17G=
ENST00000314134.3:c.535+17G= ENSP00000313318.3:n.535+17G=
ENST00000442528.2:c.496+17G= ENSP00000412408.2:n.496+17G=
NM_001145265.1:c.496+17G= NP_001138737.1:n.496+17G=
NM_001145266.1:c.496+17G= NP_001138738.1:n.496+17G=
NM_018389.4:c.535+17G= , LRG_107t1:c.535+17G= NP_060859.4:n.535+17G=
XM_011520203.1:c.535+17G= XP_011518505.1:n.535+17G=
XM_011520203.3:c.535+17G= XP_011518505.1:n.535+17G=
NM_001145265.2:c.496+17G= NP_001138737.1:n.496+17G=
NM_018389.5:c.535+17G= MANE Select NP_060859.4:n.535+17G=