Canonical Allele Identifier: CA1968692354
Gene: SLC35C1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45805820A= , CM000673.2:g.45805820A= GRCh38
NC_000011.9:g.45827371A= , CM000673.1:g.45827371A= GRCh37
NC_000011.8:g.45783947A= NCBI36
NG_009875.1:g.6749A= , LRG_107:g.6749A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526817.2:c.-21A= ENSP00000432145.2:n.-21A=
ENST00000314134.4:c.19A= MANE Select ENSP00000313318.3:p.Lys7=
ENST00000314134.3:c.19A= ENSP00000313318.3:p.Lys7=
ENST00000442528.2:c.-21A= ENSP00000412408.2:n.-21A=
ENST00000526817.1:c.-21A= ENSP00000432145.1:n.-21A=
ENST00000530471.1:c.-21A= ENSP00000432669.1:n.-21A=
NM_001145265.1:c.-21A= NP_001138737.1:n.-21A=
NM_001145266.1:c.-21A= NP_001138738.1:n.-21A=
NM_018389.4:c.19A= , LRG_107t1:c.19A= NP_060859.4:p.Lys7=
XM_011520203.1:c.19A= XP_011518505.1:p.Lys7=
XM_011520203.3:c.19A= XP_011518505.1:p.Lys7=
NM_001145265.2:c.-21A= NP_001138737.1:n.-21A=
NM_018389.5:c.19A= MANE Select NP_060859.4:p.Lys7=