Canonical Allele Identifier: CA1345477105

Gene: SLC6A1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.11031136C= , CM000665.2:g.11031136C=	GRCh38
NC_000003.11:g.11072822C= , CM000665.1:g.11072822C=	GRCh37
NC_000003.10:g.11047822C=	NCBI36
NG_053003.1:g.43408C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698198.1:c.1396-41C=	ENSP00000513602.1:n.1396-41C=
ENST00000287766.10:c.1324-41C= MANE Select	ENSP00000287766.4:n.1324-41C=
ENST00000642201.1:c.1324-41C=	ENSP00000494778.1:n.1324-41C=
ENST00000642515.1:c.1324-41C=	ENSP00000496348.1:n.1324-41C=
ENST00000642639.1:c.1324-41C=	ENSP00000494191.1:n.1324-41C=
ENST00000642735.1:c.1324-41C=	ENSP00000494050.1:n.1324-41C=
ENST00000642767.1:c.1324-41C=	ENSP00000494346.1:n.1324-41C=
ENST00000642820.1:c.1324-41C=	ENSP00000495900.1:n.1324-41C=
ENST00000643396.1:c.1324-41C=	ENSP00000494136.1:n.1324-41C=
ENST00000643498.1:c.1324-41C=	ENSP00000494997.1:n.1324-41C=
ENST00000644314.1:c.964-41C=	ENSP00000493813.1:n.964-41C=
ENST00000644803.1:c.1351-41C=	ENSP00000494469.1:n.1351-41C=
ENST00000645029.1:c.1324-41C=	ENSP00000496171.1:n.1324-41C=
ENST00000645054.1:c.1324-41C=	ENSP00000495751.1:n.1324-41C=
ENST00000645281.1:c.790-41C=	ENSP00000493746.1:n.790-41C=
ENST00000645575.1:c.*707-41C=	ENSP00000493666.1:n.*707-41C=
ENST00000645592.1:c.1324-41C=	ENSP00000496619.1:n.1324-41C=
ENST00000645776.1:c.790-41C=	ENSP00000495375.1:n.790-41C=
ENST00000645974.1:c.1324-41C=	ENSP00000496390.1:n.1324-41C=
ENST00000645985.1:c.1118-41C=
ENST00000646022.1:c.1324-41C=	ENSP00000494134.1:n.1324-41C=
ENST00000646060.1:c.1324-41C=	ENSP00000496302.1:n.1324-41C=
ENST00000646072.1:c.790-41C=	ENSP00000494002.1:n.790-41C=
ENST00000646487.1:c.901-41C=	ENSP00000496768.1:n.901-41C=
ENST00000646570.1:c.1324-41C=	ENSP00000496064.1:n.1324-41C=
ENST00000646702.1:c.1324-41C=	ENSP00000496697.1:n.1324-41C=
ENST00000646836.1:n.336C=
ENST00000646886.1:n.3692-41C=
ENST00000646924.1:c.1324-41C=	ENSP00000493591.1:n.1324-41C=
ENST00000647194.1:c.1324-41C=	ENSP00000496238.1:n.1324-41C=
ENST00000647384.1:c.1078+4777C=	ENSP00000493779.1:n.1078+4777C=
ENST00000287766.8:c.1324-41C=	ENSP00000287766.4:n.1324-41C=
NM_003042.3:c.1324-41C=	NP_003033.3:n.1324-41C=
XM_005265410.3:c.1324-41C=	XP_005265467.1:n.1324-41C=
XM_005265411.3:c.1324-41C=	XP_005265468.1:n.1324-41C=
XM_006713306.2:c.1324-41C=	XP_006713369.1:n.1324-41C=
XM_011534025.1:c.1324-41C=	XP_011532327.1:n.1324-41C=
XM_011534026.1:c.1324-41C=	XP_011532328.1:n.1324-41C=
XM_011534027.1:c.1324-41C=	XP_011532329.1:n.1324-41C=
XM_011534028.1:c.1324-41C=	XP_011532330.1:n.1324-41C=
NM_001348250.1:c.1324-41C=	NP_001335179.1:n.1324-41C=
NM_001348251.1:c.964-41C=	NP_001335180.1:n.964-41C=
NM_001348252.1:c.790-41C=	NP_001335181.1:n.790-41C=
NM_001348253.1:c.790-41C=	NP_001335182.1:n.790-41C=
XM_005265410.5:c.1324-41C=	XP_005265467.1:n.1324-41C=
XM_005265411.5:c.1324-41C=	XP_005265468.1:n.1324-41C=
XM_011534025.3:c.1324-41C=	XP_011532327.1:n.1324-41C=
XM_011534027.3:c.1324-41C=	XP_011532329.1:n.1324-41C=
XM_017007071.2:c.1324-41C=	XP_016862560.1:n.1324-41C=
XM_017007072.2:c.1324-41C=	XP_016862561.1:n.1324-41C=
NM_003042.4:c.1324-41C= MANE Select	NP_003033.3:n.1324-41C=
NM_001348250.2:c.1324-41C=	NP_001335179.1:n.1324-41C=
NM_001348251.2:c.964-41C=	NP_001335180.1:n.964-41C=
NM_001348252.2:c.790-41C=	NP_001335181.1:n.790-41C=
NM_001348253.2:c.790-41C=	NP_001335182.1:n.790-41C=