Canonical Allele Identifier: CA418437470

Gene: SLC35D1

Linked Data

• MyVariant Identifiers: chr1:g.67519691C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67054008C>T , CM000663.2:g.67054008C>T	GRCh38
NC_000001.10:g.67519691C>T , CM000663.1:g.67519691C>T	GRCh37
NC_000001.9:g.67292279C>T	NCBI36
NG_012933.1:g.5390G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.6G>A MANE Select	ENSP00000235345.5:p.Ala2=
ENST00000235345.5:c.6G>A	ENSP00000235345.5:p.Ala2=
NM_015139.2:c.6G>A	NP_055954.1:p.Ala2=
XM_006710478.1:c.6G>A	XP_006710541.1:p.Ala2=
XM_011541070.1:c.6G>A	XP_011539372.1:p.Ala2=
XM_006710478.2:c.6G>A	XP_006710541.1:p.Ala2=
XM_011541070.2:c.6G>A	XP_011539372.1:p.Ala2=
XR_001737057.2:n.416G>A
XR_001737058.2:n.409G>A
NM_015139.3:c.6G>A MANE Select	NP_055954.1:p.Ala2=