Canonical Allele Identifier: CA2613258246

Gene: SLC35C1

Linked Data

• gnomAD v4: 11-45806382-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806382T>C , CM000673.2:g.45806382T>C	GRCh38
NC_000011.9:g.45827933T>C , CM000673.1:g.45827933T>C	GRCh37
NC_000011.8:g.45784509T>C	NCBI36
NG_009875.1:g.7311T>C , LRG_107:g.7311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.496+46T>C	ENSP00000432145.2:n.496+46T>C
ENST00000314134.4:c.535+46T>C MANE Select	ENSP00000313318.3:n.535+46T>C
ENST00000314134.3:c.535+46T>C	ENSP00000313318.3:n.535+46T>C
ENST00000442528.2:c.496+46T>C	ENSP00000412408.2:n.496+46T>C
NM_001145265.1:c.496+46T>C	NP_001138737.1:n.496+46T>C
NM_001145266.1:c.496+46T>C	NP_001138738.1:n.496+46T>C
NM_018389.4:c.535+46T>C , LRG_107t1:c.535+46T>C	NP_060859.4:n.535+46T>C
XM_011520203.1:c.535+46T>C	XP_011518505.1:n.535+46T>C
XM_011520203.3:c.535+46T>C	XP_011518505.1:n.535+46T>C
NM_001145265.2:c.496+46T>C	NP_001138737.1:n.496+46T>C
NM_018389.5:c.535+46T>C MANE Select	NP_060859.4:n.535+46T>C