Canonical Allele Identifier: CA402329103

Gene: SLC14A1

Linked Data

• MyVariant Identifiers: chr18:g.43319616C>A (hg19) ; chr18:g.45739651C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45739651C>A , CM000680.2:g.45739651C>A	GRCh38
NC_000018.9:g.43319616C>A , CM000680.1:g.43319616C>A	GRCh37
NC_000018.8:g.41573614C>A	NCBI36
NG_011775.3:g.20525C>A
NG_011775.4:g.57627C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000321925.9:c.935C>A MANE Select	ENSP00000318546.4:p.Ala312Asp
ENST00000502059.7:c.*288C>A	ENSP00000442180.2:n.*288C>A
ENST00000586951.6:c.935C>A	ENSP00000465702.2:p.Ala312Asp
ENST00000588179.6:c.*265C>A	ENSP00000467898.2:n.*265C>A
ENST00000589322.7:c.539C>A	ENSP00000466273.3:p.Ala180Asp
ENST00000321925.8:c.935C>A	ENSP00000318546.4:p.Ala312Asp
ENST00000402943.6:c.620C>A	ENSP00000385320.2:p.Ala207Asp
ENST00000415427.7:c.1103C>A	ENSP00000412309.2:p.Ala368Asp
ENST00000436407.7:c.1103C>A	ENSP00000390637.2:p.Ala368Asp
ENST00000502059.6:c.611C>A	ENSP00000442180.1:p.Ala204Asp
ENST00000535474.5:c.539C>A	ENSP00000441998.1:p.Ala180Asp
ENST00000586142.5:c.935C>A	ENSP00000470476.1:p.Ala312Asp
ENST00000586854.1:n.368C>A
ENST00000588179.5:c.*265C>A	ENSP00000467898.2:n.*265C>A
ENST00000589700.5:c.787C>A	ENSP00000465044.1:p.Leu263Ile
ENST00000590377.1:c.386+3003C>A
ENST00000591541.2:n.150C>A
ENST00000619403.4:c.787C>A	ENSP00000479595.1:p.Leu263Ile
NM_001128588.3:c.1103C>A	NP_001122060.3:p.Ala368Asp
NM_001146036.2:c.935C>A	NP_001139508.2:p.Ala312Asp
NM_001146037.1:c.1103C>A	NP_001139509.1:p.Ala368Asp
NM_001308278.1:c.620C>A	NP_001295207.1:p.Ala207Asp
NM_001308279.1:c.539C>A	NP_001295208.1:p.Ala180Asp
NM_015865.6:c.935C>A	NP_056949.4:p.Ala312Asp
XM_005258329.1:c.1103C>A	XP_005258386.1:p.Ala368Asp
XM_005258333.1:c.539C>A	XP_005258390.1:p.Ala180Asp
XM_006722526.2:c.1040C>A	XP_006722589.1:p.Ala347Asp
XM_011526141.1:c.1040C>A	XP_011524443.1:p.Ala347Asp
XM_011526142.1:c.1040C>A	XP_011524444.1:p.Ala347Asp
XM_011526143.1:c.1103C>A	XP_011524445.1:p.Ala368Asp
XM_011526144.1:c.1103C>A	XP_011524446.1:p.Ala368Asp
XR_935425.1:n.680-2057G>T
NM_015865.7:c.935C>A MANE Select	NP_056949.4:p.Ala312Asp
XM_006722526.3:c.1040C>A	XP_006722589.1:p.Ala347Asp
XM_024451238.1:c.935C>A	XP_024307006.1:p.Ala312Asp
XR_001753266.1:n.1301C>A
XR_001753561.1:n.529-2057G>T
XR_935423.2:n.698-2057G>T
NM_001128588.4:c.1103C>A	NP_001122060.3:p.Ala368Asp
NM_001146036.3:c.935C>A	NP_001139508.2:p.Ala312Asp
NM_001308278.2:c.620C>A	NP_001295207.1:p.Ala207Asp
NM_001308279.2:c.539C>A	NP_001295208.1:p.Ala180Asp