Canonical Allele Identifier: CA402328851

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319526A>C (hg19) ; chr18:g.45739561A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739561A>C , CM000680.2:g.45739561A>C	GRCh38
NC_000018.9:g.43319526A>C , CM000680.1:g.43319526A>C	GRCh37
NC_000018.8:g.41573524A>C	NCBI36
NG_011775.3:g.20435A>C
NG_011775.4:g.57537A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000321925.9:c.845A>C MANE Select	ENSP00000318546.4:p.Tyr282Ser
ENST00000502059.7:c.*198A>C	ENSP00000442180.2:n.*198A>C
ENST00000586951.6:c.845A>C	ENSP00000465702.2:p.Tyr282Ser
ENST00000588179.6:c.*175A>C	ENSP00000467898.2:n.*175A>C
ENST00000589322.7:c.449A>C	ENSP00000466273.3:p.Tyr150Ser
ENST00000321925.8:c.845A>C	ENSP00000318546.4:p.Tyr282Ser
ENST00000402943.6:c.530A>C	ENSP00000385320.2:p.Tyr177Ser
ENST00000415427.7:c.1013A>C	ENSP00000412309.2:p.Tyr338Ser
ENST00000436407.7:c.1013A>C	ENSP00000390637.2:p.Tyr338Ser
ENST00000502059.6:c.521A>C	ENSP00000442180.1:p.Tyr174Ser
ENST00000535474.5:c.449A>C	ENSP00000441998.1:p.Tyr150Ser
ENST00000586142.5:c.845A>C	ENSP00000470476.1:p.Tyr282Ser
ENST00000586854.1:n.278A>C
ENST00000588179.5:c.*175A>C	ENSP00000467898.2:n.*175A>C
ENST00000589322.6:c.449A>C	ENSP00000466273.2:p.Tyr150Ser
ENST00000589700.5:c.697A>C	ENSP00000465044.1:p.Thr233Pro
ENST00000590377.1:c.386+2913A>C
ENST00000591541.2:n.60A>C
ENST00000619403.4:c.697A>C	ENSP00000479595.1:p.Thr233Pro
NM_001128588.3:c.1013A>C	NP_001122060.3:p.Tyr338Ser
NM_001146036.2:c.845A>C	NP_001139508.2:p.Tyr282Ser
NM_001146037.1:c.1013A>C	NP_001139509.1:p.Tyr338Ser
NM_001308278.1:c.530A>C	NP_001295207.1:p.Tyr177Ser
NM_001308279.1:c.449A>C	NP_001295208.1:p.Tyr150Ser
NM_015865.6:c.845A>C	NP_056949.4:p.Tyr282Ser
XM_005258329.1:c.1013A>C	XP_005258386.1:p.Tyr338Ser
XM_005258333.1:c.449A>C	XP_005258390.1:p.Tyr150Ser
XM_006722526.2:c.950A>C	XP_006722589.1:p.Tyr317Ser
XM_011526141.1:c.950A>C	XP_011524443.1:p.Tyr317Ser
XM_011526142.1:c.950A>C	XP_011524444.1:p.Tyr317Ser
XM_011526143.1:c.1013A>C	XP_011524445.1:p.Tyr338Ser
XM_011526144.1:c.1013A>C	XP_011524446.1:p.Tyr338Ser
XR_935425.1:n.680-1967T>G
NM_015865.7:c.845A>C MANE Select	NP_056949.4:p.Tyr282Ser
XM_006722526.3:c.950A>C	XP_006722589.1:p.Tyr317Ser
XM_024451238.1:c.845A>C	XP_024307006.1:p.Tyr282Ser
XR_001753266.1:n.1211A>C
XR_001753561.1:n.529-1967T>G
XR_935423.2:n.698-1967T>G
NM_001128588.4:c.1013A>C	NP_001122060.3:p.Tyr338Ser
NM_001146036.3:c.845A>C	NP_001139508.2:p.Tyr282Ser
NM_001308278.2:c.530A>C	NP_001295207.1:p.Tyr177Ser
NM_001308279.2:c.449A>C	NP_001295208.1:p.Tyr150Ser