Canonical Allele Identifier: CA402328786

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319502T>C (hg19) ; chr18:g.45739537T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739537T>C , CM000680.2:g.45739537T>C	GRCh38
NC_000018.9:g.43319502T>C , CM000680.1:g.43319502T>C	GRCh37
NC_000018.8:g.41573500T>C	NCBI36
NG_011775.3:g.20411T>C
NG_011775.4:g.57513T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.821T>C MANE Select	ENSP00000318546.4:p.Leu274Pro
ENST00000502059.7:c.*174T>C	ENSP00000442180.2:n.*174T>C
ENST00000586951.6:c.821T>C	ENSP00000465702.2:p.Leu274Pro
ENST00000588179.6:c.*151T>C	ENSP00000467898.2:n.*151T>C
ENST00000589322.7:c.425T>C	ENSP00000466273.3:p.Leu142Pro
ENST00000321925.8:c.821T>C	ENSP00000318546.4:p.Leu274Pro
ENST00000402943.6:c.506T>C	ENSP00000385320.2:p.Leu169Pro
ENST00000415427.7:c.989T>C	ENSP00000412309.2:p.Leu330Pro
ENST00000436407.7:c.989T>C	ENSP00000390637.2:p.Leu330Pro
ENST00000502059.6:c.497T>C	ENSP00000442180.1:p.Leu166Pro
ENST00000535474.5:c.425T>C	ENSP00000441998.1:p.Leu142Pro
ENST00000586142.5:c.821T>C	ENSP00000470476.1:p.Leu274Pro
ENST00000586854.1:n.254T>C
ENST00000588179.5:c.*151T>C	ENSP00000467898.2:n.*151T>C
ENST00000589322.6:c.425T>C	ENSP00000466273.2:p.Leu142Pro
ENST00000589700.5:c.673T>C	ENSP00000465044.1:p.Phe225Leu
ENST00000590377.1:c.386+2889T>C
ENST00000591541.2:n.36T>C
ENST00000619403.4:c.673T>C	ENSP00000479595.1:p.Phe225Leu
NM_001128588.3:c.989T>C	NP_001122060.3:p.Leu330Pro
NM_001146036.2:c.821T>C	NP_001139508.2:p.Leu274Pro
NM_001146037.1:c.989T>C	NP_001139509.1:p.Leu330Pro
NM_001308278.1:c.506T>C	NP_001295207.1:p.Leu169Pro
NM_001308279.1:c.425T>C	NP_001295208.1:p.Leu142Pro
NM_015865.6:c.821T>C	NP_056949.4:p.Leu274Pro
XM_005258329.1:c.989T>C	XP_005258386.1:p.Leu330Pro
XM_005258333.1:c.425T>C	XP_005258390.1:p.Leu142Pro
XM_006722526.2:c.926T>C	XP_006722589.1:p.Leu309Pro
XM_011526141.1:c.926T>C	XP_011524443.1:p.Leu309Pro
XM_011526142.1:c.926T>C	XP_011524444.1:p.Leu309Pro
XM_011526143.1:c.989T>C	XP_011524445.1:p.Leu330Pro
XM_011526144.1:c.989T>C	XP_011524446.1:p.Leu330Pro
XR_935425.1:n.680-1943A>G
NM_015865.7:c.821T>C MANE Select	NP_056949.4:p.Leu274Pro
XM_006722526.3:c.926T>C	XP_006722589.1:p.Leu309Pro
XM_024451238.1:c.821T>C	XP_024307006.1:p.Leu274Pro
XR_001753266.1:n.1187T>C
XR_001753561.1:n.529-1943A>G
XR_935423.2:n.698-1943A>G
NM_001128588.4:c.989T>C	NP_001122060.3:p.Leu330Pro
NM_001146036.3:c.821T>C	NP_001139508.2:p.Leu274Pro
NM_001308278.2:c.506T>C	NP_001295207.1:p.Leu169Pro
NM_001308279.2:c.425T>C	NP_001295208.1:p.Leu142Pro