Canonical Allele Identifier: CA402329102

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319615G>T (hg19) ; chr18:g.45739650G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739650G>T , CM000680.2:g.45739650G>T	GRCh38
NC_000018.9:g.43319615G>T , CM000680.1:g.43319615G>T	GRCh37
NC_000018.8:g.41573613G>T	NCBI36
NG_011775.3:g.20524G>T
NG_011775.4:g.57626G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.934G>T MANE Select	ENSP00000318546.4:p.Ala312Ser
ENST00000502059.7:c.*287G>T	ENSP00000442180.2:n.*287G>T
ENST00000586951.6:c.934G>T	ENSP00000465702.2:p.Ala312Ser
ENST00000588179.6:c.*264G>T	ENSP00000467898.2:n.*264G>T
ENST00000589322.7:c.538G>T	ENSP00000466273.3:p.Ala180Ser
ENST00000321925.8:c.934G>T	ENSP00000318546.4:p.Ala312Ser
ENST00000402943.6:c.619G>T	ENSP00000385320.2:p.Ala207Ser
ENST00000415427.7:c.1102G>T	ENSP00000412309.2:p.Ala368Ser
ENST00000436407.7:c.1102G>T	ENSP00000390637.2:p.Ala368Ser
ENST00000502059.6:c.610G>T	ENSP00000442180.1:p.Ala204Ser
ENST00000535474.5:c.538G>T	ENSP00000441998.1:p.Ala180Ser
ENST00000586142.5:c.934G>T	ENSP00000470476.1:p.Ala312Ser
ENST00000586854.1:n.367G>T
ENST00000588179.5:c.*264G>T	ENSP00000467898.2:n.*264G>T
ENST00000589700.5:c.786G>T	ENSP00000465044.1:p.Trp262Cys
ENST00000590377.1:c.386+3002G>T
ENST00000591541.2:n.149G>T
ENST00000619403.4:c.786G>T	ENSP00000479595.1:p.Trp262Cys
NM_001128588.3:c.1102G>T	NP_001122060.3:p.Ala368Ser
NM_001146036.2:c.934G>T	NP_001139508.2:p.Ala312Ser
NM_001146037.1:c.1102G>T	NP_001139509.1:p.Ala368Ser
NM_001308278.1:c.619G>T	NP_001295207.1:p.Ala207Ser
NM_001308279.1:c.538G>T	NP_001295208.1:p.Ala180Ser
NM_015865.6:c.934G>T	NP_056949.4:p.Ala312Ser
XM_005258329.1:c.1102G>T	XP_005258386.1:p.Ala368Ser
XM_005258333.1:c.538G>T	XP_005258390.1:p.Ala180Ser
XM_006722526.2:c.1039G>T	XP_006722589.1:p.Ala347Ser
XM_011526141.1:c.1039G>T	XP_011524443.1:p.Ala347Ser
XM_011526142.1:c.1039G>T	XP_011524444.1:p.Ala347Ser
XM_011526143.1:c.1102G>T	XP_011524445.1:p.Ala368Ser
XM_011526144.1:c.1102G>T	XP_011524446.1:p.Ala368Ser
XR_935425.1:n.680-2056C>A
NM_015865.7:c.934G>T MANE Select	NP_056949.4:p.Ala312Ser
XM_006722526.3:c.1039G>T	XP_006722589.1:p.Ala347Ser
XM_024451238.1:c.934G>T	XP_024307006.1:p.Ala312Ser
XR_001753266.1:n.1300G>T
XR_001753561.1:n.529-2056C>A
XR_935423.2:n.698-2056C>A
NM_001128588.4:c.1102G>T	NP_001122060.3:p.Ala368Ser
NM_001146036.3:c.934G>T	NP_001139508.2:p.Ala312Ser
NM_001308278.2:c.619G>T	NP_001295207.1:p.Ala207Ser
NM_001308279.2:c.538G>T	NP_001295208.1:p.Ala180Ser