Canonical Allele Identifier: CA402328763

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319494A>C (hg19) ; chr18:g.45739529A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739529A>C , CM000680.2:g.45739529A>C	GRCh38
NC_000018.9:g.43319494A>C , CM000680.1:g.43319494A>C	GRCh37
NC_000018.8:g.41573492A>C	NCBI36
NG_011775.3:g.20403A>C
NG_011775.4:g.57505A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.813A>C MANE Select	ENSP00000318546.4:p.Gly271=
ENST00000502059.7:c.*166A>C	ENSP00000442180.2:n.*166A>C
ENST00000586951.6:c.813A>C	ENSP00000465702.2:p.Gly271=
ENST00000588179.6:c.*143A>C	ENSP00000467898.2:n.*143A>C
ENST00000589322.7:c.417A>C	ENSP00000466273.3:p.Gly139=
ENST00000321925.8:c.813A>C	ENSP00000318546.4:p.Gly271=
ENST00000402943.6:c.498A>C	ENSP00000385320.2:p.Gly166=
ENST00000415427.7:c.981A>C	ENSP00000412309.2:p.Gly327=
ENST00000436407.7:c.981A>C	ENSP00000390637.2:p.Gly327=
ENST00000502059.6:c.489A>C	ENSP00000442180.1:p.Gly163=
ENST00000535474.5:c.417A>C	ENSP00000441998.1:p.Gly139=
ENST00000586142.5:c.813A>C	ENSP00000470476.1:p.Gly271=
ENST00000586854.1:n.246A>C
ENST00000588179.5:c.*143A>C	ENSP00000467898.2:n.*143A>C
ENST00000589322.6:c.417A>C	ENSP00000466273.2:p.Gly139=
ENST00000589700.5:c.665A>C	ENSP00000465044.1:p.Asp222Ala
ENST00000590377.1:c.386+2881A>C
ENST00000591541.2:n.28A>C
ENST00000619403.4:c.665A>C	ENSP00000479595.1:p.Asp222Ala
NM_001128588.3:c.981A>C	NP_001122060.3:p.Gly327=
NM_001146036.2:c.813A>C	NP_001139508.2:p.Gly271=
NM_001146037.1:c.981A>C	NP_001139509.1:p.Gly327=
NM_001308278.1:c.498A>C	NP_001295207.1:p.Gly166=
NM_001308279.1:c.417A>C	NP_001295208.1:p.Gly139=
NM_015865.6:c.813A>C	NP_056949.4:p.Gly271=
XM_005258329.1:c.981A>C	XP_005258386.1:p.Gly327=
XM_005258333.1:c.417A>C	XP_005258390.1:p.Gly139=
XM_006722526.2:c.918A>C	XP_006722589.1:p.Gly306=
XM_011526141.1:c.918A>C	XP_011524443.1:p.Gly306=
XM_011526142.1:c.918A>C	XP_011524444.1:p.Gly306=
XM_011526143.1:c.981A>C	XP_011524445.1:p.Gly327=
XM_011526144.1:c.981A>C	XP_011524446.1:p.Gly327=
XR_935425.1:n.680-1935T>G
NM_015865.7:c.813A>C MANE Select	NP_056949.4:p.Gly271=
XM_006722526.3:c.918A>C	XP_006722589.1:p.Gly306=
XM_024451238.1:c.813A>C	XP_024307006.1:p.Gly271=
XR_001753266.1:n.1179A>C
XR_001753561.1:n.529-1935T>G
XR_935423.2:n.698-1935T>G
NM_001128588.4:c.981A>C	NP_001122060.3:p.Gly327=
NM_001146036.3:c.813A>C	NP_001139508.2:p.Gly271=
NM_001308278.2:c.498A>C	NP_001295207.1:p.Gly166=
NM_001308279.2:c.417A>C	NP_001295208.1:p.Gly139=