Canonical Allele Identifier: CA1968693018
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45806131C= , CM000673.2:g.45806131C= GRCh38
NC_000011.9:g.45827682C= , CM000673.1:g.45827682C= GRCh37
NC_000011.8:g.45784258C= NCBI36
NG_009875.1:g.7060C= , LRG_107:g.7060C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.291C= ENSP00000432145.2:p.Asp97=
ENST00000314134.4:c.330C= MANE Select ENSP00000313318.3:p.Asp110=
ENST00000314134.3:c.330C= ENSP00000313318.3:p.Asp110=
ENST00000442528.2:c.291C= ENSP00000412408.2:p.Asp97=
ENST00000530471.1:c.291C= ENSP00000432669.1:p.Asp97=
NM_001145265.1:c.291C= NP_001138737.1:p.Asp97=
NM_001145266.1:c.291C= NP_001138738.1:p.Asp97=
NM_018389.4:c.330C= , LRG_107t1:c.330C= NP_060859.4:p.Asp110=
XM_011520203.1:c.330C= XP_011518505.1:p.Asp110=
XM_011520203.3:c.330C= XP_011518505.1:p.Asp110=
NM_001145265.2:c.291C= NP_001138737.1:p.Asp97=
NM_018389.5:c.330C= MANE Select NP_060859.4:p.Asp110=