Canonical Allele Identifier: CA937547681

Gene: SLC35C1

Linked Data

• dbSNP Id: rs2085865517
• gnomAD v3: 11-45805861-AG-A
• gnomAD v4: 11-45805861-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805862del , CM000673.2:g.45805862del	GRCh38
NC_000011.9:g.45827413del , CM000673.1:g.45827413del	GRCh37
NC_000011.8:g.45783989del	NCBI36
NG_009875.1:g.6791del , LRG_107:g.6791del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.22del	ENSP00000432145.2:p.Asp8ThrfsTer?
ENST00000314134.4:c.61del MANE Select	ENSP00000313318.3:p.Asp21ThrfsTer?
ENST00000314134.3:c.61del	ENSP00000313318.3:p.Asp21ThrfsTer?
ENST00000442528.2:c.22del	ENSP00000412408.2:p.Asp8ThrfsTer?
ENST00000526817.1:c.22del	ENSP00000432145.1:p.Asp8ThrfsTer?
ENST00000530471.1:c.22del	ENSP00000432669.1:p.Asp8ThrfsTer?
NM_001145265.1:c.22del	NP_001138737.1:p.Asp8ThrfsTer?
NM_001145266.1:c.22del	NP_001138738.1:p.Asp8ThrfsTer?
NM_018389.4:c.61del , LRG_107t1:c.61del	NP_060859.4:p.Asp21ThrfsTer?
XM_011520203.1:c.61del	XP_011518505.1:p.Asp21ThrfsTer?
XM_011520203.3:c.61del	XP_011518505.1:p.Asp21ThrfsTer?
NM_001145265.2:c.22del	NP_001138737.1:p.Asp8ThrfsTer?
NM_018389.5:c.61del MANE Select	NP_060859.4:p.Asp21ThrfsTer?