Canonical Allele Identifier: CA1144699873

Gene: SLC6A9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.44000787C= , CM000663.2:g.44000787C=	GRCh38
NC_000001.10:g.44466459C= , CM000663.1:g.44466459C=	GRCh37
NC_000001.9:g.44239046C=	NCBI36
NG_050929.1:g.35706G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372310.8:c.1516G= MANE Select	ENSP00000361384.4:p.Val506=
ENST00000673836.1:c.1516G=	ENSP00000501314.1:p.Val506=
ENST00000357730.6:c.1573G=	ENSP00000350362.2:p.Val525=
ENST00000360584.6:c.1735G=	ENSP00000353791.2:p.Val579=
ENST00000372306.7:c.1604G=	ENSP00000361380.3:p.Arg535=
ENST00000372307.7:c.1321G=	ENSP00000361381.3:p.Val441=
ENST00000372310.7:c.1516G=	ENSP00000361384.3:p.Val506=
ENST00000475075.6:c.1183G=	ENSP00000434460.1:p.Val395=
NM_001024845.2:c.1516G=	NP_001020016.1:p.Val506=
NM_001261380.1:c.1528G=	NP_001248309.1:p.Val510=
NM_006934.3:c.1573G=	NP_008865.2:p.Val525=
NM_201649.3:c.1735G=	NP_964012.2:p.Val579=
NR_048548.1:n.1776G=
NR_048549.1:n.1499G=
XM_011542017.1:c.1735G=	XP_011540319.1:p.Val579=
NM_001328626.1:c.1183G=	NP_001315555.1:p.Val395=
NM_001328627.1:c.1453G=	NP_001315556.1:p.Val485=
NM_001328628.1:c.1321G=	NP_001315557.1:p.Val441=
NM_001328629.1:c.1516G=	NP_001315558.1:p.Val506=
NM_001328630.1:c.1183G=	NP_001315559.1:p.Val395=
XM_011542017.2:c.1735G=	XP_011540319.1:p.Val579=
XM_017002152.2:c.1435G=	XP_016857641.1:p.Val479=
XM_017002153.2:c.1402G=	XP_016857642.1:p.Val468=
XM_024449295.1:c.1321G=	XP_024305063.1:p.Val441=
NM_001024845.3:c.1516G= MANE Select	NP_001020016.1:p.Val506=
NM_001261380.2:c.1528G=	NP_001248309.1:p.Val510=
NM_001328626.2:c.1183G=	NP_001315555.1:p.Val395=
NM_001328630.2:c.1183G=	NP_001315559.1:p.Val395=
NM_006934.4:c.1573G=	NP_008865.2:p.Val525=
NM_201649.4:c.1735G=	NP_964012.2:p.Val579=
NR_048548.2:n.1599G=