Canonical Allele Identifier: CA402328843

Gene: SLC14A1

Linked Data

• dbSNP Id: rs775333866
• gnomAD v3: 18-45739558-T-C
• gnomAD v4: 18-45739558-T-C
• MyVariant Identifiers: chr18:g.43319523T>C (hg19) ; chr18:g.45739558T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739558T>C , CM000680.2:g.45739558T>C	GRCh38
NC_000018.9:g.43319523T>C , CM000680.1:g.43319523T>C	GRCh37
NC_000018.8:g.41573521T>C	NCBI36
NG_011775.3:g.20432T>C
NG_011775.4:g.57534T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000321925.9:c.842T>C MANE Select	ENSP00000318546.4:p.Ile281Thr
ENST00000502059.7:c.*195T>C	ENSP00000442180.2:n.*195T>C
ENST00000586951.6:c.842T>C	ENSP00000465702.2:p.Ile281Thr
ENST00000588179.6:c.*172T>C	ENSP00000467898.2:n.*172T>C
ENST00000589322.7:c.446T>C	ENSP00000466273.3:p.Ile149Thr
ENST00000321925.8:c.842T>C	ENSP00000318546.4:p.Ile281Thr
ENST00000402943.6:c.527T>C	ENSP00000385320.2:p.Ile176Thr
ENST00000415427.7:c.1010T>C	ENSP00000412309.2:p.Ile337Thr
ENST00000436407.7:c.1010T>C	ENSP00000390637.2:p.Ile337Thr
ENST00000502059.6:c.518T>C	ENSP00000442180.1:p.Ile173Thr
ENST00000535474.5:c.446T>C	ENSP00000441998.1:p.Ile149Thr
ENST00000586142.5:c.842T>C	ENSP00000470476.1:p.Ile281Thr
ENST00000586854.1:n.275T>C
ENST00000588179.5:c.*172T>C	ENSP00000467898.2:n.*172T>C
ENST00000589322.6:c.446T>C	ENSP00000466273.2:p.Ile149Thr
ENST00000589700.5:c.694T>C	ENSP00000465044.1:p.Ser232Pro
ENST00000590377.1:c.386+2910T>C
ENST00000591541.2:n.57T>C
ENST00000619403.4:c.694T>C	ENSP00000479595.1:p.Ser232Pro
NM_001128588.3:c.1010T>C	NP_001122060.3:p.Ile337Thr
NM_001146036.2:c.842T>C	NP_001139508.2:p.Ile281Thr
NM_001146037.1:c.1010T>C	NP_001139509.1:p.Ile337Thr
NM_001308278.1:c.527T>C	NP_001295207.1:p.Ile176Thr
NM_001308279.1:c.446T>C	NP_001295208.1:p.Ile149Thr
NM_015865.6:c.842T>C	NP_056949.4:p.Ile281Thr
XM_005258329.1:c.1010T>C	XP_005258386.1:p.Ile337Thr
XM_005258333.1:c.446T>C	XP_005258390.1:p.Ile149Thr
XM_006722526.2:c.947T>C	XP_006722589.1:p.Ile316Thr
XM_011526141.1:c.947T>C	XP_011524443.1:p.Ile316Thr
XM_011526142.1:c.947T>C	XP_011524444.1:p.Ile316Thr
XM_011526143.1:c.1010T>C	XP_011524445.1:p.Ile337Thr
XM_011526144.1:c.1010T>C	XP_011524446.1:p.Ile337Thr
XR_935425.1:n.680-1964A>G
NM_015865.7:c.842T>C MANE Select	NP_056949.4:p.Ile281Thr
XM_006722526.3:c.947T>C	XP_006722589.1:p.Ile316Thr
XM_024451238.1:c.842T>C	XP_024307006.1:p.Ile281Thr
XR_001753266.1:n.1208T>C
XR_001753561.1:n.529-1964A>G
XR_935423.2:n.698-1964A>G
NM_001128588.4:c.1010T>C	NP_001122060.3:p.Ile337Thr
NM_001146036.3:c.842T>C	NP_001139508.2:p.Ile281Thr
NM_001308278.2:c.527T>C	NP_001295207.1:p.Ile176Thr
NM_001308279.2:c.446T>C	NP_001295208.1:p.Ile149Thr