Canonical Allele Identifier: CA474036646

Gene: SLC35C1

Linked Data

• dbSNP Id: rs1406492802
• gnomAD v2: 11-45827739-C-T
• MyVariant Identifiers: chr11:g.45827739C>T (hg19) ; chr11:g.45806188C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806188C>T , CM000673.2:g.45806188C>T	GRCh38
NC_000011.9:g.45827739C>T , CM000673.1:g.45827739C>T	GRCh37
NC_000011.8:g.45784315C>T	NCBI36
NG_009875.1:g.7117C>T , LRG_107:g.7117C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.348C>T	ENSP00000432145.2:p.Thr116=
ENST00000314134.4:c.387C>T MANE Select	ENSP00000313318.3:p.Thr129=
ENST00000314134.3:c.387C>T	ENSP00000313318.3:p.Thr129=
ENST00000442528.2:c.348C>T	ENSP00000412408.2:p.Thr116=
ENST00000530471.1:c.348C>T	ENSP00000432669.1:p.Thr116=
NM_001145265.1:c.348C>T	NP_001138737.1:p.Thr116=
NM_001145266.1:c.348C>T	NP_001138738.1:p.Thr116=
NM_018389.4:c.387C>T , LRG_107t1:c.387C>T	NP_060859.4:p.Thr129=
XM_011520203.1:c.387C>T	XP_011518505.1:p.Thr129=
XM_011520203.3:c.387C>T	XP_011518505.1:p.Thr129=
NM_001145265.2:c.348C>T	NP_001138737.1:p.Thr116=
NM_018389.5:c.387C>T MANE Select	NP_060859.4:p.Thr129=