Canonical Allele Identifier: CA1172961725

Gene: SLC35D1

Linked Data

• dbSNP Id: rs1169782082

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67009365G>T , CM000663.2:g.67009365G>T	GRCh38
NC_000001.10:g.67475048G>T , CM000663.1:g.67475048G>T	GRCh37
NC_000001.9:g.67247636G>T	NCBI36
NG_012933.1:g.50033C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235345.6:c.877-198C>A MANE Select	ENSP00000235345.5:n.877-198C>A
ENST00000235345.5:c.877-198C>A	ENSP00000235345.5:n.877-198C>A
NM_015139.2:c.877-198C>A	NP_055954.1:n.877-198C>A
XM_006710478.1:c.958-198C>A	XP_006710541.1:n.958-198C>A
XM_011541070.1:c.958-198C>A	XP_011539372.1:n.958-198C>A
XM_006710478.2:c.958-198C>A	XP_006710541.1:n.958-198C>A
XM_011541070.2:c.958-198C>A	XP_011539372.1:n.958-198C>A
XR_001737057.2:n.1461-198C>A
XR_001737058.2:n.2246-198C>A
NM_015139.3:c.877-198C>A MANE Select	NP_055954.1:n.877-198C>A