Canonical Allele Identifier: CA418437428

Gene: SLC35D1

Linked Data

• MyVariant Identifiers: chr1:g.67519664C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053981C>T , CM000663.2:g.67053981C>T	GRCh38
NC_000001.10:g.67519664C>T , CM000663.1:g.67519664C>T	GRCh37
NC_000001.9:g.67292252C>T	NCBI36
NG_012933.1:g.5417G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.33G>A MANE Select	ENSP00000235345.5:p.Arg11=
ENST00000235345.5:c.33G>A	ENSP00000235345.5:p.Arg11=
NM_015139.2:c.33G>A	NP_055954.1:p.Arg11=
XM_006710478.1:c.33G>A	XP_006710541.1:p.Arg11=
XM_011541070.1:c.33G>A	XP_011539372.1:p.Arg11=
XM_006710478.2:c.33G>A	XP_006710541.1:p.Arg11=
XM_011541070.2:c.33G>A	XP_011539372.1:p.Arg11=
XR_001737057.2:n.443G>A
XR_001737058.2:n.436G>A
NM_015139.3:c.33G>A MANE Select	NP_055954.1:p.Arg11=