Canonical Allele Identifier: CA474036364

Gene: SLC35C1

Linked Data

• ClinVar Variation Id: 2788772
• ClinVar RCV Id: RCV003611841
• dbSNP Id: rs1326280684
• MyVariant Identifiers: chr11:g.45827418C>T (hg19) ; chr11:g.45805867C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805867C>T , CM000673.2:g.45805867C>T	GRCh38
NC_000011.9:g.45827418C>T , CM000673.1:g.45827418C>T	GRCh37
NC_000011.8:g.45783994C>T	NCBI36
NG_009875.1:g.6796C>T , LRG_107:g.6796C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.27C>T	ENSP00000432145.2:p.Pro9=
ENST00000314134.4:c.66C>T MANE Select	ENSP00000313318.3:p.Pro22=
ENST00000314134.3:c.66C>T	ENSP00000313318.3:p.Pro22=
ENST00000442528.2:c.27C>T	ENSP00000412408.2:p.Pro9=
ENST00000526817.1:c.27C>T	ENSP00000432145.1:p.Pro9=
ENST00000530471.1:c.27C>T	ENSP00000432669.1:p.Pro9=
NM_001145265.1:c.27C>T	NP_001138737.1:p.Pro9=
NM_001145266.1:c.27C>T	NP_001138738.1:p.Pro9=
NM_018389.4:c.66C>T , LRG_107t1:c.66C>T	NP_060859.4:p.Pro22=
XM_011520203.1:c.66C>T	XP_011518505.1:p.Pro22=
XM_011520203.3:c.66C>T	XP_011518505.1:p.Pro22=
NM_001145265.2:c.27C>T	NP_001138737.1:p.Pro9=
NM_018389.5:c.66C>T MANE Select	NP_060859.4:p.Pro22=