Canonical Allele Identifier: CA418437356
Gene: SLC35D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67519562G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053879G>T , CM000663.2:g.67053879G>T GRCh38
NC_000001.10:g.67519562G>T , CM000663.1:g.67519562G>T GRCh37
NC_000001.9:g.67292150G>T NCBI36
NG_012933.1:g.5519C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.135C>A MANE Select ENSP00000235345.5:p.Ala45=
ENST00000235345.5:c.135C>A ENSP00000235345.5:p.Ala45=
NM_015139.2:c.135C>A NP_055954.1:p.Ala45=
XM_006710478.1:c.135C>A XP_006710541.1:p.Ala45=
XM_011541070.1:c.135C>A XP_011539372.1:p.Ala45=
XM_006710478.2:c.135C>A XP_006710541.1:p.Ala45=
XM_011541070.2:c.135C>A XP_011539372.1:p.Ala45=
XR_001737057.2:n.545C>A
XR_001737058.2:n.538C>A
NM_015139.3:c.135C>A MANE Select NP_055954.1:p.Ala45=