Canonical Allele Identifier: CA299688315

Gene: SLC14A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45651657G>A , CM000680.2:g.45651657G>A	GRCh38
NC_000018.9:g.43231622G>A , CM000680.1:g.43231622G>A	GRCh37
NC_000018.8:g.41485620G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255226.11:c.1351+7497G>A MANE Select	ENSP00000255226.5:n.1351+7497G>A
ENST00000255226.10:c.1351+7497G>A	ENSP00000255226.5:n.1351+7497G>A
ENST00000586448.5:c.1351+7497G>A	ENSP00000465953.1:n.1351+7497G>A
ENST00000589658.5:c.1351+7497G>A	ENSP00000465349.2:n.1351+7497G>A
NM_001242692.1:c.1351+7497G>A	NP_001229621.1:n.1351+7497G>A
NM_007163.3:c.1351+7497G>A	NP_009094.3:n.1351+7497G>A
XM_011526216.1:c.1351+7497G>A	XP_011524518.1:n.1351+7497G>A
XM_011526217.1:c.1216+7497G>A	XP_011524519.1:n.1216+7497G>A
XM_017026016.2:c.1216+7497G>A	XP_016881505.1:n.1216+7497G>A
XM_024451270.1:c.1351+7497G>A	XP_024307038.1:n.1351+7497G>A
XM_024451271.1:c.1351+7497G>A	XP_024307039.1:n.1351+7497G>A
XR_935423.2:n.873-14500C>T
NM_001242692.2:c.1351+7497G>A	NP_001229621.1:n.1351+7497G>A
NM_001371319.1:c.1351+7497G>A	NP_001358248.1:n.1351+7497G>A
NM_007163.4:c.1351+7497G>A MANE Select	NP_009094.3:n.1351+7497G>A