Canonical Allele Identifier: CA402328859

Gene: SLC14A1

Linked Data

• dbSNP Id: rs2047296903
• MyVariant Identifiers: chr18:g.43319529T>A (hg19) ; chr18:g.45739564T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739564T>A , CM000680.2:g.45739564T>A	GRCh38
NC_000018.9:g.43319529T>A , CM000680.1:g.43319529T>A	GRCh37
NC_000018.8:g.41573527T>A	NCBI36
NG_011775.3:g.20438T>A
NG_011775.4:g.57540T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.848T>A MANE Select	ENSP00000318546.4:p.Phe283Tyr
ENST00000502059.7:c.*201T>A	ENSP00000442180.2:n.*201T>A
ENST00000586951.6:c.848T>A	ENSP00000465702.2:p.Phe283Tyr
ENST00000588179.6:c.*178T>A	ENSP00000467898.2:n.*178T>A
ENST00000589322.7:c.452T>A	ENSP00000466273.3:p.Phe151Tyr
ENST00000321925.8:c.848T>A	ENSP00000318546.4:p.Phe283Tyr
ENST00000402943.6:c.533T>A	ENSP00000385320.2:p.Phe178Tyr
ENST00000415427.7:c.1016T>A	ENSP00000412309.2:p.Phe339Tyr
ENST00000436407.7:c.1016T>A	ENSP00000390637.2:p.Phe339Tyr
ENST00000502059.6:c.524T>A	ENSP00000442180.1:p.Phe175Tyr
ENST00000535474.5:c.452T>A	ENSP00000441998.1:p.Phe151Tyr
ENST00000586142.5:c.848T>A	ENSP00000470476.1:p.Phe283Tyr
ENST00000586854.1:n.281T>A
ENST00000588179.5:c.*178T>A	ENSP00000467898.2:n.*178T>A
ENST00000589322.6:c.452T>A	ENSP00000466273.2:p.Phe151Tyr
ENST00000589700.5:c.700T>A	ENSP00000465044.1:p.Leu234Met
ENST00000590377.1:c.386+2916T>A
ENST00000591541.2:n.63T>A
ENST00000619403.4:c.700T>A	ENSP00000479595.1:p.Leu234Met
NM_001128588.3:c.1016T>A	NP_001122060.3:p.Phe339Tyr
NM_001146036.2:c.848T>A	NP_001139508.2:p.Phe283Tyr
NM_001146037.1:c.1016T>A	NP_001139509.1:p.Phe339Tyr
NM_001308278.1:c.533T>A	NP_001295207.1:p.Phe178Tyr
NM_001308279.1:c.452T>A	NP_001295208.1:p.Phe151Tyr
NM_015865.6:c.848T>A	NP_056949.4:p.Phe283Tyr
XM_005258329.1:c.1016T>A	XP_005258386.1:p.Phe339Tyr
XM_005258333.1:c.452T>A	XP_005258390.1:p.Phe151Tyr
XM_006722526.2:c.953T>A	XP_006722589.1:p.Phe318Tyr
XM_011526141.1:c.953T>A	XP_011524443.1:p.Phe318Tyr
XM_011526142.1:c.953T>A	XP_011524444.1:p.Phe318Tyr
XM_011526143.1:c.1016T>A	XP_011524445.1:p.Phe339Tyr
XM_011526144.1:c.1016T>A	XP_011524446.1:p.Phe339Tyr
XR_935425.1:n.680-1970A>T
NM_015865.7:c.848T>A MANE Select	NP_056949.4:p.Phe283Tyr
XM_006722526.3:c.953T>A	XP_006722589.1:p.Phe318Tyr
XM_024451238.1:c.848T>A	XP_024307006.1:p.Phe283Tyr
XR_001753266.1:n.1214T>A
XR_001753561.1:n.529-1970A>T
XR_935423.2:n.698-1970A>T
NM_001128588.4:c.1016T>A	NP_001122060.3:p.Phe339Tyr
NM_001146036.3:c.848T>A	NP_001139508.2:p.Phe283Tyr
NM_001308278.2:c.533T>A	NP_001295207.1:p.Phe178Tyr
NM_001308279.2:c.452T>A	NP_001295208.1:p.Phe151Tyr