Canonical Allele Identifier: CA13016015

Gene: SLC35D2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.96369762C>T , CM000671.2:g.96369762C>T	GRCh38
NC_000009.11:g.99132044C>T , CM000671.1:g.99132044C>T	GRCh37
NC_000009.10:g.98171865C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253270.13:c.159-1457G>A MANE Select	ENSP00000253270.7:n.159-1457G>A
ENST00000375257.2:c.159-1457G>A	ENSP00000364406.1:n.159-1457G>A
ENST00000375259.9:c.159-1457G>A	ENSP00000364408.4:n.159-1457G>A
ENST00000482643.2:n.288-1457G>A
ENST00000253270.11:c.159-1457G>A	ENSP00000253270.7:n.159-1457G>A
ENST00000375257.1:c.159-1457G>A	ENSP00000364406.1:n.159-1457G>A
ENST00000375259.8:c.159-1457G>A	ENSP00000364408.4:n.159-1457G>A
ENST00000482643.1:n.288-1457G>A
NM_001286990.1:c.159-1457G>A	NP_001273919.1:n.159-1457G>A
NM_007001.2:c.159-1457G>A	NP_008932.2:n.159-1457G>A
NR_104627.1:n.235-1457G>A
XM_005251673.1:c.159-1457G>A	XP_005251730.1:n.159-1457G>A
XM_005251674.1:c.159-1457G>A	XP_005251731.1:n.159-1457G>A
XM_005251675.2:c.159-1457G>A	XP_005251732.1:n.159-1457G>A
XM_005251676.1:c.159-1457G>A	XP_005251733.1:n.159-1457G>A
XM_006716939.2:c.159-1457G>A	XP_006717002.1:n.159-1457G>A
XM_011518164.1:c.159-1457G>A	XP_011516466.1:n.159-1457G>A
XM_011518165.1:c.-34-1457G>A	XP_011516467.1:n.-34-1457G>A
XR_929705.1:n.210-1457G>A
XR_001746170.1:n.220-1457G>A
NM_007001.3:c.159-1457G>A MANE Select	NP_008932.2:n.159-1457G>A
NM_001286990.2:c.159-1457G>A	NP_001273919.1:n.159-1457G>A
NR_104627.2:n.236-1457G>A