Canonical Allele Identifier: CA418437385

Gene: SLC35D1

Linked Data

• MyVariant Identifiers: chr1:g.67519595G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67053912G>C , CM000663.2:g.67053912G>C	GRCh38
NC_000001.10:g.67519595G>C , CM000663.1:g.67519595G>C	GRCh37
NC_000001.9:g.67292183G>C	NCBI36
NG_012933.1:g.5486C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.102C>G MANE Select	ENSP00000235345.5:p.Ala34=
ENST00000235345.5:c.102C>G	ENSP00000235345.5:p.Ala34=
NM_015139.2:c.102C>G	NP_055954.1:p.Ala34=
XM_006710478.1:c.102C>G	XP_006710541.1:p.Ala34=
XM_011541070.1:c.102C>G	XP_011539372.1:p.Ala34=
XM_006710478.2:c.102C>G	XP_006710541.1:p.Ala34=
XM_011541070.2:c.102C>G	XP_011539372.1:p.Ala34=
XR_001737057.2:n.512C>G
XR_001737058.2:n.505C>G
NM_015139.3:c.102C>G MANE Select	NP_055954.1:p.Ala34=