Canonical Allele Identifier: CA418437412

Gene: SLC35D1

Linked Data

• MyVariant Identifiers: chr1:g.67519634G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053951G>T , CM000663.2:g.67053951G>T	GRCh38
NC_000001.10:g.67519634G>T , CM000663.1:g.67519634G>T	GRCh37
NC_000001.9:g.67292222G>T	NCBI36
NG_012933.1:g.5447C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.63C>A MANE Select	ENSP00000235345.5:p.Ser21=
ENST00000235345.5:c.63C>A	ENSP00000235345.5:p.Ser21=
NM_015139.2:c.63C>A	NP_055954.1:p.Ser21=
XM_006710478.1:c.63C>A	XP_006710541.1:p.Ser21=
XM_011541070.1:c.63C>A	XP_011539372.1:p.Ser21=
XM_006710478.2:c.63C>A	XP_006710541.1:p.Ser21=
XM_011541070.2:c.63C>A	XP_011539372.1:p.Ser21=
XR_001737057.2:n.473C>A
XR_001737058.2:n.466C>A
NM_015139.3:c.63C>A MANE Select	NP_055954.1:p.Ser21=