Canonical Allele Identifier: CA402329048

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319595C>G (hg19) ; chr18:g.45739630C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739630C>G , CM000680.2:g.45739630C>G	GRCh38
NC_000018.9:g.43319595C>G , CM000680.1:g.43319595C>G	GRCh37
NC_000018.8:g.41573593C>G	NCBI36
NG_011775.3:g.20504C>G
NG_011775.4:g.57606C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.914C>G MANE Select	ENSP00000318546.4:p.Thr305Ser
ENST00000502059.7:c.*267C>G	ENSP00000442180.2:n.*267C>G
ENST00000586951.6:c.914C>G	ENSP00000465702.2:p.Thr305Ser
ENST00000588179.6:c.*244C>G	ENSP00000467898.2:n.*244C>G
ENST00000589322.7:c.518C>G	ENSP00000466273.3:p.Thr173Ser
ENST00000321925.8:c.914C>G	ENSP00000318546.4:p.Thr305Ser
ENST00000402943.6:c.599C>G	ENSP00000385320.2:p.Thr200Ser
ENST00000415427.7:c.1082C>G	ENSP00000412309.2:p.Thr361Ser
ENST00000436407.7:c.1082C>G	ENSP00000390637.2:p.Thr361Ser
ENST00000502059.6:c.590C>G	ENSP00000442180.1:p.Thr197Ser
ENST00000535474.5:c.518C>G	ENSP00000441998.1:p.Thr173Ser
ENST00000586142.5:c.914C>G	ENSP00000470476.1:p.Thr305Ser
ENST00000586854.1:n.347C>G
ENST00000588179.5:c.*244C>G	ENSP00000467898.2:n.*244C>G
ENST00000589700.5:c.766C>G	ENSP00000465044.1:p.Pro256Ala
ENST00000590377.1:c.386+2982C>G
ENST00000591541.2:n.129C>G
ENST00000619403.4:c.766C>G	ENSP00000479595.1:p.Pro256Ala
NM_001128588.3:c.1082C>G	NP_001122060.3:p.Thr361Ser
NM_001146036.2:c.914C>G	NP_001139508.2:p.Thr305Ser
NM_001146037.1:c.1082C>G	NP_001139509.1:p.Thr361Ser
NM_001308278.1:c.599C>G	NP_001295207.1:p.Thr200Ser
NM_001308279.1:c.518C>G	NP_001295208.1:p.Thr173Ser
NM_015865.6:c.914C>G	NP_056949.4:p.Thr305Ser
XM_005258329.1:c.1082C>G	XP_005258386.1:p.Thr361Ser
XM_005258333.1:c.518C>G	XP_005258390.1:p.Thr173Ser
XM_006722526.2:c.1019C>G	XP_006722589.1:p.Thr340Ser
XM_011526141.1:c.1019C>G	XP_011524443.1:p.Thr340Ser
XM_011526142.1:c.1019C>G	XP_011524444.1:p.Thr340Ser
XM_011526143.1:c.1082C>G	XP_011524445.1:p.Thr361Ser
XM_011526144.1:c.1082C>G	XP_011524446.1:p.Thr361Ser
XR_935425.1:n.680-2036G>C
NM_015865.7:c.914C>G MANE Select	NP_056949.4:p.Thr305Ser
XM_006722526.3:c.1019C>G	XP_006722589.1:p.Thr340Ser
XM_024451238.1:c.914C>G	XP_024307006.1:p.Thr305Ser
XR_001753266.1:n.1280C>G
XR_001753561.1:n.529-2036G>C
XR_935423.2:n.698-2036G>C
NM_001128588.4:c.1082C>G	NP_001122060.3:p.Thr361Ser
NM_001146036.3:c.914C>G	NP_001139508.2:p.Thr305Ser
NM_001308278.2:c.599C>G	NP_001295207.1:p.Thr200Ser
NM_001308279.2:c.518C>G	NP_001295208.1:p.Thr173Ser