Canonical Allele Identifier: CA340067653

Gene: SLC6A9

Linked Data

• MyVariant Identifiers: chr1:g.44466483A>C (hg19) ; chr1:g.44000811A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44000811A>C , CM000663.2:g.44000811A>C	GRCh38
NC_000001.10:g.44466483A>C , CM000663.1:g.44466483A>C	GRCh37
NC_000001.9:g.44239070A>C	NCBI36
NG_050929.1:g.35682T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372310.8:c.1492T>G MANE Select	ENSP00000361384.4:p.Phe498Val
ENST00000673836.1:c.1492T>G	ENSP00000501314.1:p.Phe498Val
ENST00000357730.6:c.1549T>G	ENSP00000350362.2:p.Phe517Val
ENST00000360584.6:c.1711T>G	ENSP00000353791.2:p.Phe571Val
ENST00000372306.7:c.1580T>G	ENSP00000361380.3:p.Leu527Arg
ENST00000372307.7:c.1297T>G	ENSP00000361381.3:p.Phe433Val
ENST00000372310.7:c.1492T>G	ENSP00000361384.3:p.Phe498Val
ENST00000475075.6:c.1159T>G	ENSP00000434460.1:p.Phe387Val
NM_001024845.2:c.1492T>G	NP_001020016.1:p.Phe498Val
NM_001261380.1:c.1504T>G	NP_001248309.1:p.Phe502Val
NM_006934.3:c.1549T>G	NP_008865.2:p.Phe517Val
NM_201649.3:c.1711T>G	NP_964012.2:p.Phe571Val
NR_048548.1:n.1752T>G
NR_048549.1:n.1475T>G
XM_011542017.1:c.1711T>G	XP_011540319.1:p.Phe571Val
NM_001328626.1:c.1159T>G	NP_001315555.1:p.Phe387Val
NM_001328627.1:c.1429T>G	NP_001315556.1:p.Phe477Val
NM_001328628.1:c.1297T>G	NP_001315557.1:p.Phe433Val
NM_001328629.1:c.1492T>G	NP_001315558.1:p.Phe498Val
NM_001328630.1:c.1159T>G	NP_001315559.1:p.Phe387Val
XM_011542017.2:c.1711T>G	XP_011540319.1:p.Phe571Val
XM_017002152.2:c.1411T>G	XP_016857641.1:p.Phe471Val
XM_017002153.2:c.1378T>G	XP_016857642.1:p.Phe460Val
XM_024449295.1:c.1297T>G	XP_024305063.1:p.Phe433Val
NM_001024845.3:c.1492T>G MANE Select	NP_001020016.1:p.Phe498Val
NM_001261380.2:c.1504T>G	NP_001248309.1:p.Phe502Val
NM_001328626.2:c.1159T>G	NP_001315555.1:p.Phe387Val
NM_001328630.2:c.1159T>G	NP_001315559.1:p.Phe387Val
NM_006934.4:c.1549T>G	NP_008865.2:p.Phe517Val
NM_201649.4:c.1711T>G	NP_964012.2:p.Phe571Val
NR_048548.2:n.1575T>G