Canonical Allele Identifier: CA1630848666
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805799A= , CM000673.2:g.45805799A= GRCh38
NC_000011.9:g.45827350A= , CM000673.1:g.45827350A= GRCh37
NC_000011.8:g.45783926A= NCBI36
NG_009875.1:g.6728A= , LRG_107:g.6728A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.-31-11A= ENSP00000432145.2:n.-31-11A=
ENST00000314134.4:c.-3A= MANE Select ENSP00000313318.3:n.-3A=
ENST00000314134.3:c.-3A= ENSP00000313318.3:n.-3A=
ENST00000442528.2:c.-31-11A= ENSP00000412408.2:n.-31-11A=
ENST00000526817.1:c.-31-11A= ENSP00000432145.1:n.-31-11A=
ENST00000530471.1:c.-31-11A= ENSP00000432669.1:n.-31-11A=
NM_001145265.1:c.-31-11A= NP_001138737.1:n.-31-11A=
NM_001145266.1:c.-31-11A= NP_001138738.1:n.-31-11A=
NM_018389.4:c.-3A= , LRG_107t1:c.-3A= NP_060859.4:n.-3A=
XM_011520203.1:c.-3A= XP_011518505.1:n.-3A=
XM_011520203.3:c.-3A= XP_011518505.1:n.-3A=
NM_001145265.2:c.-31-11A= NP_001138737.1:n.-31-11A=
NM_018389.5:c.-3A= MANE Select NP_060859.4:n.-3A=