Canonical Allele Identifier: CA2613258197

Gene: SLC35C1

Linked Data

• gnomAD v4: 11-45805815-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805816del , CM000673.2:g.45805816del	GRCh38
NC_000011.9:g.45827367del , CM000673.1:g.45827367del	GRCh37
NC_000011.8:g.45783943del	NCBI36
NG_009875.1:g.6745del , LRG_107:g.6745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.-25del	ENSP00000432145.2:n.-25del
ENST00000314134.4:c.15del MANE Select	ENSP00000313318.3:p.Leu6Ter
ENST00000314134.3:c.15del	ENSP00000313318.3:p.Leu6Ter
ENST00000442528.2:c.-25del	ENSP00000412408.2:n.-25del
ENST00000526817.1:c.-25del	ENSP00000432145.1:n.-25del
ENST00000530471.1:c.-25del	ENSP00000432669.1:n.-25del
NM_001145265.1:c.-25del	NP_001138737.1:n.-25del
NM_001145266.1:c.-25del	NP_001138738.1:n.-25del
NM_018389.4:c.15del , LRG_107t1:c.15del	NP_060859.4:p.Leu6Ter
XM_011520203.1:c.15del	XP_011518505.1:p.Leu6Ter
XM_011520203.3:c.15del	XP_011518505.1:p.Leu6Ter
NM_001145265.2:c.-25del	NP_001138737.1:n.-25del
NM_018389.5:c.15del MANE Select	NP_060859.4:p.Leu6Ter