Canonical Allele Identifier: CA402328762

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319493G>C (hg19) ; chr18:g.45739528G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739528G>C , CM000680.2:g.45739528G>C	GRCh38
NC_000018.9:g.43319493G>C , CM000680.1:g.43319493G>C	GRCh37
NC_000018.8:g.41573491G>C	NCBI36
NG_011775.3:g.20402G>C
NG_011775.4:g.57504G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.812G>C MANE Select	ENSP00000318546.4:p.Gly271Ala
ENST00000502059.7:c.*165G>C	ENSP00000442180.2:n.*165G>C
ENST00000586951.6:c.812G>C	ENSP00000465702.2:p.Gly271Ala
ENST00000588179.6:c.*142G>C	ENSP00000467898.2:n.*142G>C
ENST00000589322.7:c.416G>C	ENSP00000466273.3:p.Gly139Ala
ENST00000321925.8:c.812G>C	ENSP00000318546.4:p.Gly271Ala
ENST00000402943.6:c.497G>C	ENSP00000385320.2:p.Gly166Ala
ENST00000415427.7:c.980G>C	ENSP00000412309.2:p.Gly327Ala
ENST00000436407.7:c.980G>C	ENSP00000390637.2:p.Gly327Ala
ENST00000502059.6:c.488G>C	ENSP00000442180.1:p.Gly163Ala
ENST00000535474.5:c.416G>C	ENSP00000441998.1:p.Gly139Ala
ENST00000586142.5:c.812G>C	ENSP00000470476.1:p.Gly271Ala
ENST00000586854.1:n.245G>C
ENST00000588179.5:c.*142G>C	ENSP00000467898.2:n.*142G>C
ENST00000589322.6:c.416G>C	ENSP00000466273.2:p.Gly139Ala
ENST00000589700.5:c.664G>C	ENSP00000465044.1:p.Asp222His
ENST00000590377.1:c.386+2880G>C
ENST00000591541.2:n.27G>C
ENST00000619403.4:c.664G>C	ENSP00000479595.1:p.Asp222His
NM_001128588.3:c.980G>C	NP_001122060.3:p.Gly327Ala
NM_001146036.2:c.812G>C	NP_001139508.2:p.Gly271Ala
NM_001146037.1:c.980G>C	NP_001139509.1:p.Gly327Ala
NM_001308278.1:c.497G>C	NP_001295207.1:p.Gly166Ala
NM_001308279.1:c.416G>C	NP_001295208.1:p.Gly139Ala
NM_015865.6:c.812G>C	NP_056949.4:p.Gly271Ala
XM_005258329.1:c.980G>C	XP_005258386.1:p.Gly327Ala
XM_005258333.1:c.416G>C	XP_005258390.1:p.Gly139Ala
XM_006722526.2:c.917G>C	XP_006722589.1:p.Gly306Ala
XM_011526141.1:c.917G>C	XP_011524443.1:p.Gly306Ala
XM_011526142.1:c.917G>C	XP_011524444.1:p.Gly306Ala
XM_011526143.1:c.980G>C	XP_011524445.1:p.Gly327Ala
XM_011526144.1:c.980G>C	XP_011524446.1:p.Gly327Ala
XR_935425.1:n.680-1934C>G
NM_015865.7:c.812G>C MANE Select	NP_056949.4:p.Gly271Ala
XM_006722526.3:c.917G>C	XP_006722589.1:p.Gly306Ala
XM_024451238.1:c.812G>C	XP_024307006.1:p.Gly271Ala
XR_001753266.1:n.1178G>C
XR_001753561.1:n.529-1934C>G
XR_935423.2:n.698-1934C>G
NM_001128588.4:c.980G>C	NP_001122060.3:p.Gly327Ala
NM_001146036.3:c.812G>C	NP_001139508.2:p.Gly271Ala
NM_001308278.2:c.497G>C	NP_001295207.1:p.Gly166Ala
NM_001308279.2:c.416G>C	NP_001295208.1:p.Gly139Ala