Canonical Allele Identifier: CA402328805

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319508C>T (hg19) ; chr18:g.45739543C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739543C>T , CM000680.2:g.45739543C>T	GRCh38
NC_000018.9:g.43319508C>T , CM000680.1:g.43319508C>T	GRCh37
NC_000018.8:g.41573506C>T	NCBI36
NG_011775.3:g.20417C>T
NG_011775.4:g.57519C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.827C>T MANE Select	ENSP00000318546.4:p.Ala276Val
ENST00000502059.7:c.*180C>T	ENSP00000442180.2:n.*180C>T
ENST00000586951.6:c.827C>T	ENSP00000465702.2:p.Ala276Val
ENST00000588179.6:c.*157C>T	ENSP00000467898.2:n.*157C>T
ENST00000589322.7:c.431C>T	ENSP00000466273.3:p.Ala144Val
ENST00000321925.8:c.827C>T	ENSP00000318546.4:p.Ala276Val
ENST00000402943.6:c.512C>T	ENSP00000385320.2:p.Ala171Val
ENST00000415427.7:c.995C>T	ENSP00000412309.2:p.Ala332Val
ENST00000436407.7:c.995C>T	ENSP00000390637.2:p.Ala332Val
ENST00000502059.6:c.503C>T	ENSP00000442180.1:p.Ala168Val
ENST00000535474.5:c.431C>T	ENSP00000441998.1:p.Ala144Val
ENST00000586142.5:c.827C>T	ENSP00000470476.1:p.Ala276Val
ENST00000586854.1:n.260C>T
ENST00000588179.5:c.*157C>T	ENSP00000467898.2:n.*157C>T
ENST00000589322.6:c.431C>T	ENSP00000466273.2:p.Ala144Val
ENST00000589700.5:c.679C>T	ENSP00000465044.1:p.Pro227Ser
ENST00000590377.1:c.386+2895C>T
ENST00000591541.2:n.42C>T
ENST00000619403.4:c.679C>T	ENSP00000479595.1:p.Pro227Ser
NM_001128588.3:c.995C>T	NP_001122060.3:p.Ala332Val
NM_001146036.2:c.827C>T	NP_001139508.2:p.Ala276Val
NM_001146037.1:c.995C>T	NP_001139509.1:p.Ala332Val
NM_001308278.1:c.512C>T	NP_001295207.1:p.Ala171Val
NM_001308279.1:c.431C>T	NP_001295208.1:p.Ala144Val
NM_015865.6:c.827C>T	NP_056949.4:p.Ala276Val
XM_005258329.1:c.995C>T	XP_005258386.1:p.Ala332Val
XM_005258333.1:c.431C>T	XP_005258390.1:p.Ala144Val
XM_006722526.2:c.932C>T	XP_006722589.1:p.Ala311Val
XM_011526141.1:c.932C>T	XP_011524443.1:p.Ala311Val
XM_011526142.1:c.932C>T	XP_011524444.1:p.Ala311Val
XM_011526143.1:c.995C>T	XP_011524445.1:p.Ala332Val
XM_011526144.1:c.995C>T	XP_011524446.1:p.Ala332Val
XR_935425.1:n.680-1949G>A
NM_015865.7:c.827C>T MANE Select	NP_056949.4:p.Ala276Val
XM_006722526.3:c.932C>T	XP_006722589.1:p.Ala311Val
XM_024451238.1:c.827C>T	XP_024307006.1:p.Ala276Val
XR_001753266.1:n.1193C>T
XR_001753561.1:n.529-1949G>A
XR_935423.2:n.698-1949G>A
NM_001128588.4:c.995C>T	NP_001122060.3:p.Ala332Val
NM_001146036.3:c.827C>T	NP_001139508.2:p.Ala276Val
NM_001308278.2:c.512C>T	NP_001295207.1:p.Ala171Val
NM_001308279.2:c.431C>T	NP_001295208.1:p.Ala144Val