Canonical Allele Identifier: CA10638618

Gene: SLC35C1

Linked Data

• ClinVar Variation Id: 304732
• ClinVar RCV Id: RCV000326613
• dbSNP Id: rs886048313
• MyVariant Identifiers: chr11:g.45827119T>G (hg19) ; chr11:g.45805568T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45805568T>G , CM000673.2:g.45805568T>G	GRCh38
NC_000011.9:g.45827119T>G , CM000673.1:g.45827119T>G	GRCh37
NC_000011.8:g.45783695T>G	NCBI36
NG_009875.1:g.6497T>G , LRG_107:g.6497T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.-31-242T>G	ENSP00000432145.2:n.-31-242T>G
ENST00000314134.4:c.-234T>G MANE Select	ENSP00000313318.3:n.-234T>G
ENST00000314134.3:c.-234T>G	ENSP00000313318.3:n.-234T>G
ENST00000442528.2:c.-31-242T>G	ENSP00000412408.2:n.-31-242T>G
ENST00000526817.1:c.-31-242T>G	ENSP00000432145.1:n.-31-242T>G
ENST00000530471.1:c.-31-242T>G	ENSP00000432669.1:n.-31-242T>G
NM_001145265.1:c.-31-242T>G	NP_001138737.1:n.-31-242T>G
NM_001145266.1:c.-31-242T>G	NP_001138738.1:n.-31-242T>G
NM_018389.4:c.-234T>G , LRG_107t1:c.-234T>G	NP_060859.4:n.-234T>G
XM_011520203.1:c.-234T>G	XP_011518505.1:n.-234T>G
XM_011520203.3:c.-234T>G	XP_011518505.1:n.-234T>G
NM_001145265.2:c.-31-242T>G	NP_001138737.1:n.-31-242T>G
NM_018389.5:c.-234T>G MANE Select	NP_060859.4:n.-234T>G