Canonical Allele Identifier: CA2300515629

Gene: SLC14A1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739489_45739490delinsGC , CM000680.2:g.45739489_45739490delinsGC	GRCh38
NC_000018.9:g.43319454_43319455delinsGC , CM000680.1:g.43319454_43319455delinsGC	GRCh37
NC_000018.8:g.41573452_41573453delinsGC	NCBI36
NG_011775.3:g.20363_20364delinsGC
NG_011775.4:g.57465_57466delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000321925.9:c.812-39_812-38delinsGC MANE Select	ENSP00000318546.4:n.812-39_812-38delinsGC...
ENST00000502059.7:c.*165-39_*165-38delinsGC	ENSP00000442180.2:n.*165-39_*165-38delins...
ENST00000586951.6:c.812-39_812-38delinsGC	ENSP00000465702.2:n.812-39_812-38delinsGC...
ENST00000588179.6:c.*142-39_*142-38delinsGC	ENSP00000467898.2:n.*142-39_*142-38delins...
ENST00000589322.7:c.416-39_416-38delinsGC	ENSP00000466273.3:n.416-39_416-38delinsGC...
ENST00000321925.8:c.812-39_812-38delinsGC	ENSP00000318546.4:n.812-39_812-38delinsGC...
ENST00000402943.6:c.497-39_497-38delinsGC	ENSP00000385320.2:n.497-39_497-38delinsGC...
ENST00000415427.7:c.980-39_980-38delinsGC	ENSP00000412309.2:n.980-39_980-38delinsGC...
ENST00000436407.7:c.980-39_980-38delinsGC	ENSP00000390637.2:n.980-39_980-38delinsGC...
ENST00000502059.6:c.488-39_488-38delinsGC	ENSP00000442180.1:n.488-39_488-38delinsGC...
ENST00000535474.5:c.416-39_416-38delinsGC	ENSP00000441998.1:n.416-39_416-38delinsGC...
ENST00000586142.5:c.812-39_812-38delinsGC	ENSP00000470476.1:n.812-39_812-38delinsGC...
ENST00000586854.1:n.245-39_245-38delinsGC
ENST00000588179.5:c.*142-39_*142-38delinsGC	ENSP00000467898.2:n.*142-39_*142-38delins...
ENST00000589322.6:c.416-39_416-38delinsGC	ENSP00000466273.2:n.416-39_416-38delinsGC...
ENST00000589700.5:c.664-39_664-38delinsGC	ENSP00000465044.1:n.664-39_664-38delinsGC...
ENST00000590377.1:c.386+2841_386+2842delinsGC
ENST00000619403.4:c.664-39_664-38delinsGC	ENSP00000479595.1:n.664-39_664-38delinsGC...
NM_001128588.3:c.980-39_980-38delinsGC	NP_001122060.3:n.980-39_980-38delinsGC
NM_001146036.2:c.812-39_812-38delinsGC	NP_001139508.2:n.812-39_812-38delinsGC
NM_001146037.1:c.980-39_980-38delinsGC	NP_001139509.1:n.980-39_980-38delinsGC
NM_001308278.1:c.497-39_497-38delinsGC	NP_001295207.1:n.497-39_497-38delinsGC
NM_001308279.1:c.416-39_416-38delinsGC	NP_001295208.1:n.416-39_416-38delinsGC
NM_015865.6:c.812-39_812-38delinsGC	NP_056949.4:n.812-39_812-38delinsGC
XM_005258329.1:c.980-39_980-38delinsGC	XP_005258386.1:n.980-39_980-38delinsGC
XM_005258333.1:c.416-39_416-38delinsGC	XP_005258390.1:n.416-39_416-38delinsGC
XM_006722526.2:c.917-39_917-38delinsGC	XP_006722589.1:n.917-39_917-38delinsGC
XM_011526141.1:c.917-39_917-38delinsGC	XP_011524443.1:n.917-39_917-38delinsGC
XM_011526142.1:c.917-39_917-38delinsGC	XP_011524444.1:n.917-39_917-38delinsGC
XM_011526143.1:c.980-39_980-38delinsGC	XP_011524445.1:n.980-39_980-38delinsGC
XM_011526144.1:c.980-39_980-38delinsGC	XP_011524446.1:n.980-39_980-38delinsGC
XR_935425.1:n.680-1896_680-1895delinsGC
NM_015865.7:c.812-39_812-38delinsGC MANE Select	NP_056949.4:n.812-39_812-38delinsGC
XM_006722526.3:c.917-39_917-38delinsGC	XP_006722589.1:n.917-39_917-38delinsGC
XM_024451238.1:c.812-39_812-38delinsGC	XP_024307006.1:n.812-39_812-38delinsGC
XR_001753266.1:n.1178-39_1178-38delinsGC
XR_001753561.1:n.529-1896_529-1895delinsGC
XR_935423.2:n.698-1896_698-1895delinsGC
NM_001128588.4:c.980-39_980-38delinsGC	NP_001122060.3:n.980-39_980-38delinsGC
NM_001146036.3:c.812-39_812-38delinsGC	NP_001139508.2:n.812-39_812-38delinsGC
NM_001308278.2:c.497-39_497-38delinsGC	NP_001295207.1:n.497-39_497-38delinsGC
NM_001308279.2:c.416-39_416-38delinsGC	NP_001295208.1:n.416-39_416-38delinsGC