Canonical Allele Identifier: CA2011409176

Gene: SLC6A13

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.242627A= , CM000674.2:g.242627A=	GRCh38
NC_000012.11:g.351793A= , CM000674.1:g.351793A=	GRCh37
NC_000012.10:g.222054A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343164.9:c.465T= MANE Select	ENSP00000339260.4:p.His155=
ENST00000343164.8:c.465T=	ENSP00000339260.4:p.His155=
ENST00000445055.6:c.203-4617T=	ENSP00000407104.2:n.203-4617T=
ENST00000536842.5:n.518T=
ENST00000539260.1:c.*104T=	ENSP00000437386.1:n.*104T=
ENST00000542272.5:c.108T=	ENSP00000443466.1:p.His36=
ENST00000546319.5:c.203-4617T=	ENSP00000444606.1:n.203-4617T=
NM_001190997.2:c.203-4617T=	NP_001177926.1:n.203-4617T=
NM_016615.4:c.465T=	NP_057699.2:p.His155=
XM_005253749.2:c.531T=	XP_005253806.1:p.His177=
XM_011521012.1:c.108T=	XP_011519314.1:p.His36=
XM_011521013.1:c.-195T=	XP_011519315.1:n.-195T=
XM_011521014.1:c.-195T=	XP_011519316.1:n.-195T=
XM_011521012.2:c.108T=	XP_011519314.1:p.His36=
XM_017019844.1:c.465T=	XP_016875333.1:p.His155=
XM_017019846.1:c.465T=	XP_016875335.1:p.His155=
XM_017019847.1:c.465T=	XP_016875336.1:p.His155=
XR_001748849.1:n.518T=
XR_002957372.1:n.518T=
NM_016615.5:c.465T= MANE Select	NP_057699.2:p.His155=
NM_001190997.3:c.203-4617T=	NP_001177926.1:n.203-4617T=