Canonical Allele Identifier: CA899188

Gene: SLC35D1

Linked Data

• dbSNP Id: rs745328042
• ExAC: 1:67519637 G / T
• gnomAD v2: 1-67519637-G-T
• gnomAD v4: 1-67053954-G-T
• MyVariant Identifiers: chr1:g.67519637G>T (hg19) ; chr1:g.67053954G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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