Canonical Allele Identifier: CA418437362

Gene: SLC35D1

Linked Data

• MyVariant Identifiers: chr1:g.67519568C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053885C>A , CM000663.2:g.67053885C>A	GRCh38
NC_000001.10:g.67519568C>A , CM000663.1:g.67519568C>A	GRCh37
NC_000001.9:g.67292156C>A	NCBI36
NG_012933.1:g.5513G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.129G>T MANE Select	ENSP00000235345.5:p.Leu43=
ENST00000235345.5:c.129G>T	ENSP00000235345.5:p.Leu43=
NM_015139.2:c.129G>T	NP_055954.1:p.Leu43=
XM_006710478.1:c.129G>T	XP_006710541.1:p.Leu43=
XM_011541070.1:c.129G>T	XP_011539372.1:p.Leu43=
XM_006710478.2:c.129G>T	XP_006710541.1:p.Leu43=
XM_011541070.2:c.129G>T	XP_011539372.1:p.Leu43=
XR_001737057.2:n.539G>T
XR_001737058.2:n.532G>T
NM_015139.3:c.129G>T MANE Select	NP_055954.1:p.Leu43=