Canonical Allele Identifier: CA24005530

Gene: SLC35D1

Linked Data

• dbSNP Id: rs926288200
• MyVariant Identifiers: chr1:g.67474725A>T (hg19) ; chr1:g.67009042A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009042A>T , CM000663.2:g.67009042A>T	GRCh38
NC_000001.10:g.67474725A>T , CM000663.1:g.67474725A>T	GRCh37
NC_000001.9:g.67247313A>T	NCBI36
NG_012933.1:g.50356T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.959+43T>A MANE Select	ENSP00000235345.5:n.959+43T>A
ENST00000235345.5:c.959+43T>A	ENSP00000235345.5:n.959+43T>A
NM_015139.2:c.959+43T>A	NP_055954.1:n.959+43T>A
XM_006710478.1:c.1040+43T>A	XP_006710541.1:n.1040+43T>A
XM_011541070.1:c.1040+43T>A	XP_011539372.1:n.1040+43T>A
XM_006710478.2:c.1040+43T>A	XP_006710541.1:n.1040+43T>A
XM_011541070.2:c.1040+43T>A	XP_011539372.1:n.1040+43T>A
XR_001737057.2:n.1543+43T>A
XR_001737058.2:n.2328+43T>A
NM_015139.3:c.959+43T>A MANE Select	NP_055954.1:n.959+43T>A