Canonical Allele Identifier: CA738078821

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1231014771
• gnomAD v3: 1-67054126-C-T
• gnomAD v4: 1-67054126-C-T
• MyVariant Identifiers: chr1:g.67519809C>T (hg19) ; chr1:g.67054126C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054126C>T , CM000663.2:g.67054126C>T	GRCh38
NC_000001.10:g.67519809C>T , CM000663.1:g.67519809C>T	GRCh37
NC_000001.9:g.67292397C>T	NCBI36
NG_012933.1:g.5272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.-113G>A MANE Select	ENSP00000235345.5:n.-113G>A
NM_015139.2:c.-113G>A	NP_055954.1:n.-113G>A
XM_006710478.1:c.-113G>A	XP_006710541.1:n.-113G>A
XM_011541070.1:c.-113G>A	XP_011539372.1:n.-113G>A
XM_006710478.2:c.-113G>A	XP_006710541.1:n.-113G>A
XM_011541070.2:c.-113G>A	XP_011539372.1:n.-113G>A
XR_001737057.2:n.298G>A
XR_001737058.2:n.291G>A
NM_015139.3:c.-113G>A MANE Select	NP_055954.1:n.-113G>A