Canonical Allele Identifier: CA418437387
Gene: SLC35D1 HGNC NCBI

Linked Data

gnomAD v4: 1-67053915-C-G
MyVariant Identifiers: chr1:g.67519598C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053915C>G , CM000663.2:g.67053915C>G GRCh38
NC_000001.10:g.67519598C>G , CM000663.1:g.67519598C>G GRCh37
NC_000001.9:g.67292186C>G NCBI36
NG_012933.1:g.5483G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.99G>C MANE Select ENSP00000235345.5:p.Ser33=
ENST00000235345.5:c.99G>C ENSP00000235345.5:p.Ser33=
NM_015139.2:c.99G>C NP_055954.1:p.Ser33=
XM_006710478.1:c.99G>C XP_006710541.1:p.Ser33=
XM_011541070.1:c.99G>C XP_011539372.1:p.Ser33=
XM_006710478.2:c.99G>C XP_006710541.1:p.Ser33=
XM_011541070.2:c.99G>C XP_011539372.1:p.Ser33=
XR_001737057.2:n.509G>C
XR_001737058.2:n.502G>C
NM_015139.3:c.99G>C MANE Select NP_055954.1:p.Ser33=