Canonical Allele Identifier: CA2595957453
Gene: SLC35C1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805748_45805750del , CM000673.2:g.45805748_45805750del GRCh38
NC_000011.9:g.45827299_45827301del , CM000673.1:g.45827299_45827301del GRCh37
NC_000011.8:g.45783875_45783877del NCBI36
NG_009875.1:g.6677_6679del , LRG_107:g.6677_6679del

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.-31-62_-31-60del ENSP00000432145.2:n.-31-62_-31-60del
ENST00000314134.4:c.-54_-52del MANE Select ENSP00000313318.3:n.-54_-52del
ENST00000314134.3:c.-54_-52del ENSP00000313318.3:n.-54_-52del
ENST00000442528.2:c.-31-62_-31-60del ENSP00000412408.2:n.-31-62_-31-60del
ENST00000526817.1:c.-31-62_-31-60del ENSP00000432145.1:n.-31-62_-31-60del
ENST00000530471.1:c.-31-62_-31-60del ENSP00000432669.1:n.-31-62_-31-60del
NM_001145265.1:c.-31-62_-31-60del NP_001138737.1:n.-31-62_-31-60del
NM_001145266.1:c.-31-62_-31-60del NP_001138738.1:n.-31-62_-31-60del
NM_018389.4:c.-54_-52del , LRG_107t1:c.-54_-52del NP_060859.4:n.-54_-52del
XM_011520203.1:c.-54_-52del XP_011518505.1:n.-54_-52del
XM_011520203.3:c.-54_-52del XP_011518505.1:n.-54_-52del
NM_001145265.2:c.-31-62_-31-60del NP_001138737.1:n.-31-62_-31-60del
NM_018389.5:c.-54_-52del MANE Select NP_060859.4:n.-54_-52del