Canonical Allele Identifier: CA676889897

Gene: SLC35C1

Linked Data

• dbSNP Id: rs1394520710
• gnomAD v3: 11-45806367-A-G
• gnomAD v4: 11-45806367-A-G
• MyVariant Identifiers: chr11:g.45827918A>G (hg19) ; chr11:g.45806367A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.45806367A>G , CM000673.2:g.45806367A>G	GRCh38
NC_000011.9:g.45827918A>G , CM000673.1:g.45827918A>G	GRCh37
NC_000011.8:g.45784494A>G	NCBI36
NG_009875.1:g.7296A>G , LRG_107:g.7296A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526817.2:c.496+31A>G	ENSP00000432145.2:n.496+31A>G
ENST00000314134.4:c.535+31A>G MANE Select	ENSP00000313318.3:n.535+31A>G
ENST00000314134.3:c.535+31A>G	ENSP00000313318.3:n.535+31A>G
ENST00000442528.2:c.496+31A>G	ENSP00000412408.2:n.496+31A>G
NM_001145265.1:c.496+31A>G	NP_001138737.1:n.496+31A>G
NM_001145266.1:c.496+31A>G	NP_001138738.1:n.496+31A>G
NM_018389.4:c.535+31A>G , LRG_107t1:c.535+31A>G	NP_060859.4:n.535+31A>G
XM_011520203.1:c.535+31A>G	XP_011518505.1:n.535+31A>G
XM_011520203.3:c.535+31A>G	XP_011518505.1:n.535+31A>G
NM_001145265.2:c.496+31A>G	NP_001138737.1:n.496+31A>G
NM_018389.5:c.535+31A>G MANE Select	NP_060859.4:n.535+31A>G