Canonical Allele Identifier: CA1968692933

Gene: SLC35C1

Linked Data

• dbSNP Id: rs2085869545
• gnomAD v4: 11-45806031-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806034_45806036del , CM000673.2:g.45806034_45806036del	GRCh38
NC_000011.9:g.45827585_45827587del , CM000673.1:g.45827585_45827587del	GRCh37
NC_000011.8:g.45784161_45784163del	NCBI36
NG_009875.1:g.6963_6965del , LRG_107:g.6963_6965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.194_196del	ENSP00000432145.2:p.Phe65del
ENST00000314134.4:c.233_235del MANE Select	ENSP00000313318.3:p.Phe78del
ENST00000314134.3:c.233_235del	ENSP00000313318.3:p.Phe78del
ENST00000442528.2:c.194_196del	ENSP00000412408.2:p.Phe65del
ENST00000526817.1:c.194_196del	ENSP00000432145.1:p.Phe65del
ENST00000530471.1:c.194_196del	ENSP00000432669.1:p.Phe65del
NM_001145265.1:c.194_196del	NP_001138737.1:p.Phe65del
NM_001145266.1:c.194_196del	NP_001138738.1:p.Phe65del
NM_018389.4:c.233_235del , LRG_107t1:c.233_235del	NP_060859.4:p.Phe78del
XM_011520203.1:c.233_235del	XP_011518505.1:p.Phe78del
XM_011520203.3:c.233_235del	XP_011518505.1:p.Phe78del
NM_001145265.2:c.194_196del	NP_001138737.1:p.Phe65del
NM_018389.5:c.233_235del MANE Select	NP_060859.4:p.Phe78del