Canonical Allele Identifier: CA1968692264
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805775G= , CM000673.2:g.45805775G= GRCh38
NC_000011.9:g.45827326G= , CM000673.1:g.45827326G= GRCh37
NC_000011.8:g.45783902G= NCBI36
NG_009875.1:g.6704G= , LRG_107:g.6704G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.-31-35G= ENSP00000432145.2:n.-31-35G=
ENST00000314134.4:c.-27G= MANE Select ENSP00000313318.3:n.-27G=
ENST00000314134.3:c.-27G= ENSP00000313318.3:n.-27G=
ENST00000442528.2:c.-31-35G= ENSP00000412408.2:n.-31-35G=
ENST00000526817.1:c.-31-35G= ENSP00000432145.1:n.-31-35G=
ENST00000530471.1:c.-31-35G= ENSP00000432669.1:n.-31-35G=
NM_001145265.1:c.-31-35G= NP_001138737.1:n.-31-35G=
NM_001145266.1:c.-31-35G= NP_001138738.1:n.-31-35G=
NM_018389.4:c.-27G= , LRG_107t1:c.-27G= NP_060859.4:n.-27G=
XM_011520203.1:c.-27G= XP_011518505.1:n.-27G=
XM_011520203.3:c.-27G= XP_011518505.1:n.-27G=
NM_001145265.2:c.-31-35G= NP_001138737.1:n.-31-35G=
NM_018389.5:c.-27G= MANE Select NP_060859.4:n.-27G=