Canonical Allele Identifier: CA402328908
Gene: SLC14A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.45739580C>A , CM000680.2:g.45739580C>A GRCh38
NC_000018.9:g.43319545C>A , CM000680.1:g.43319545C>A GRCh37
NC_000018.8:g.41573543C>A NCBI36
NG_011775.3:g.20454C>A
NG_011775.4:g.57556C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000321925.9:c.864C>A MANE Select ENSP00000318546.4:p.Phe288Leu
ENST00000502059.7:c.*217C>A ENSP00000442180.2:n.*217C>A
ENST00000586951.6:c.864C>A ENSP00000465702.2:p.Phe288Leu
ENST00000588179.6:c.*194C>A ENSP00000467898.2:n.*194C>A
ENST00000589322.7:c.468C>A ENSP00000466273.3:p.Phe156Leu
ENST00000321925.8:c.864C>A ENSP00000318546.4:p.Phe288Leu
ENST00000402943.6:c.549C>A ENSP00000385320.2:p.Phe183Leu
ENST00000415427.7:c.1032C>A ENSP00000412309.2:p.Phe344Leu
ENST00000436407.7:c.1032C>A ENSP00000390637.2:p.Phe344Leu
ENST00000502059.6:c.540C>A ENSP00000442180.1:p.Phe180Leu
ENST00000535474.5:c.468C>A ENSP00000441998.1:p.Phe156Leu
ENST00000586142.5:c.864C>A ENSP00000470476.1:p.Phe288Leu
ENST00000586854.1:n.297C>A
ENST00000588179.5:c.*194C>A ENSP00000467898.2:n.*194C>A
ENST00000589322.6:c.468C>A ENSP00000466273.2:p.Phe156Leu
ENST00000589700.5:c.716C>A ENSP00000465044.1:p.Ser239Ter
ENST00000590377.1:c.386+2932C>A
ENST00000591541.2:n.79C>A
ENST00000619403.4:c.716C>A ENSP00000479595.1:p.Ser239Ter
NM_001128588.3:c.1032C>A NP_001122060.3:p.Phe344Leu
NM_001146036.2:c.864C>A NP_001139508.2:p.Phe288Leu
NM_001146037.1:c.1032C>A NP_001139509.1:p.Phe344Leu
NM_001308278.1:c.549C>A NP_001295207.1:p.Phe183Leu
NM_001308279.1:c.468C>A NP_001295208.1:p.Phe156Leu
NM_015865.6:c.864C>A NP_056949.4:p.Phe288Leu
XM_005258329.1:c.1032C>A XP_005258386.1:p.Phe344Leu
XM_005258333.1:c.468C>A XP_005258390.1:p.Phe156Leu
XM_006722526.2:c.969C>A XP_006722589.1:p.Phe323Leu
XM_011526141.1:c.969C>A XP_011524443.1:p.Phe323Leu
XM_011526142.1:c.969C>A XP_011524444.1:p.Phe323Leu
XM_011526143.1:c.1032C>A XP_011524445.1:p.Phe344Leu
XM_011526144.1:c.1032C>A XP_011524446.1:p.Phe344Leu
XR_935425.1:n.680-1986G>T
NM_015865.7:c.864C>A MANE Select NP_056949.4:p.Phe288Leu
XM_006722526.3:c.969C>A XP_006722589.1:p.Phe323Leu
XM_024451238.1:c.864C>A XP_024307006.1:p.Phe288Leu
XR_001753266.1:n.1230C>A
XR_001753561.1:n.529-1986G>T
XR_935423.2:n.698-1986G>T
NM_001128588.4:c.1032C>A NP_001122060.3:p.Phe344Leu
NM_001146036.3:c.864C>A NP_001139508.2:p.Phe288Leu
NM_001308278.2:c.549C>A NP_001295207.1:p.Phe183Leu
NM_001308279.2:c.468C>A NP_001295208.1:p.Phe156Leu