Canonical Allele Identifier: CA418232914

Gene: SLC35D1

Linked Data

• MyVariant Identifiers: chr1:g.67474791T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009108T>G , CM000663.2:g.67009108T>G	GRCh38
NC_000001.10:g.67474791T>G , CM000663.1:g.67474791T>G	GRCh37
NC_000001.9:g.67247379T>G	NCBI36
NG_012933.1:g.50290A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.936A>C MANE Select	ENSP00000235345.5:p.Thr312=
ENST00000235345.5:c.936A>C	ENSP00000235345.5:p.Thr312=
NM_015139.2:c.936A>C	NP_055954.1:p.Thr312=
XM_006710478.1:c.1017A>C	XP_006710541.1:p.Thr339=
XM_011541070.1:c.1017A>C	XP_011539372.1:p.Thr339=
XM_006710478.2:c.1017A>C	XP_006710541.1:p.Thr339=
XM_011541070.2:c.1017A>C	XP_011539372.1:p.Thr339=
XR_001737057.2:n.1520A>C
XR_001737058.2:n.2305A>C
NM_015139.3:c.936A>C MANE Select	NP_055954.1:p.Thr312=