Canonical Allele Identifier: CA418437414
Gene: SLC35D1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.67519637G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053954G>A , CM000663.2:g.67053954G>A GRCh38
NC_000001.10:g.67519637G>A , CM000663.1:g.67519637G>A GRCh37
NC_000001.9:g.67292225G>A NCBI36
NG_012933.1:g.5444C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.60C>T MANE Select ENSP00000235345.5:p.Ser20=
ENST00000235345.5:c.60C>T ENSP00000235345.5:p.Ser20=
NM_015139.2:c.60C>T NP_055954.1:p.Ser20=
XM_006710478.1:c.60C>T XP_006710541.1:p.Ser20=
XM_011541070.1:c.60C>T XP_011539372.1:p.Ser20=
XM_006710478.2:c.60C>T XP_006710541.1:p.Ser20=
XM_011541070.2:c.60C>T XP_011539372.1:p.Ser20=
XR_001737057.2:n.470C>T
XR_001737058.2:n.463C>T
NM_015139.3:c.60C>T MANE Select NP_055954.1:p.Ser20=