Canonical Allele Identifier: CA2613258195

Gene: SLC35C1

Linked Data

• gnomAD v4: 11-45805809-G-GCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805809_45805810insCAT , CM000673.2:g.45805809_45805810insCAT	GRCh38
NC_000011.9:g.45827360_45827361insCAT , CM000673.1:g.45827360_45827361insCAT	GRCh37
NC_000011.8:g.45783936_45783937insCAT	NCBI36
NG_009875.1:g.6738_6739insCAT , LRG_107:g.6738_6739insCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.-31-1_-31insCAT	ENSP00000432145.2:n.-31-1_-31insCAT
ENST00000314134.4:c.8_9insCAT MANE Select	ENSP00000313318.3:p.Arg3delinsSerMet
ENST00000314134.3:c.8_9insCAT	ENSP00000313318.3:p.Arg3delinsSerMet
ENST00000442528.2:c.-31-1_-31insCAT	ENSP00000412408.2:n.-31-1_-31insCAT
ENST00000526817.1:c.-31-1_-31insCAT	ENSP00000432145.1:n.-31-1_-31insCAT
ENST00000530471.1:c.-31-1_-31insCAT	ENSP00000432669.1:n.-31-1_-31insCAT
NM_001145265.1:c.-31-1_-31insCAT	NP_001138737.1:n.-31-1_-31insCAT
NM_001145266.1:c.-31-1_-31insCAT	NP_001138738.1:n.-31-1_-31insCAT
NM_018389.4:c.8_9insCAT , LRG_107t1:c.8_9insCAT	NP_060859.4:p.Arg3delinsSerMet
XM_011520203.1:c.8_9insCAT	XP_011518505.1:p.Arg3delinsSerMet
XM_011520203.3:c.8_9insCAT	XP_011518505.1:p.Arg3delinsSerMet
NM_001145265.2:c.-31-1_-31insCAT	NP_001138737.1:n.-31-1_-31insCAT
NM_018389.5:c.8_9insCAT MANE Select	NP_060859.4:p.Arg3delinsSerMet