Canonical Allele Identifier: CA2011409191

Gene: SLC6A13

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.242638C= , CM000674.2:g.242638C=	GRCh38
NC_000012.11:g.351804C= , CM000674.1:g.351804C=	GRCh37
NC_000012.10:g.222065C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343164.9:c.454G= MANE Select	ENSP00000339260.4:p.Gly152=
ENST00000343164.8:c.454G=	ENSP00000339260.4:p.Gly152=
ENST00000445055.6:c.203-4628G=	ENSP00000407104.2:n.203-4628G=
ENST00000536842.5:n.507G=
ENST00000539260.1:c.*93G=	ENSP00000437386.1:n.*93G=
ENST00000542272.5:c.97G=	ENSP00000443466.1:p.Gly33=
ENST00000546319.5:c.203-4628G=	ENSP00000444606.1:n.203-4628G=
NM_001190997.2:c.203-4628G=	NP_001177926.1:n.203-4628G=
NM_016615.4:c.454G=	NP_057699.2:p.Gly152=
XM_005253749.2:c.520G=	XP_005253806.1:p.Gly174=
XM_011521012.1:c.97G=	XP_011519314.1:p.Gly33=
XM_011521013.1:c.-206G=	XP_011519315.1:n.-206G=
XM_011521014.1:c.-206G=	XP_011519316.1:n.-206G=
XM_011521012.2:c.97G=	XP_011519314.1:p.Gly33=
XM_017019844.1:c.454G=	XP_016875333.1:p.Gly152=
XM_017019846.1:c.454G=	XP_016875335.1:p.Gly152=
XM_017019847.1:c.454G=	XP_016875336.1:p.Gly152=
XR_001748849.1:n.507G=
XR_002957372.1:n.507G=
NM_016615.5:c.454G= MANE Select	NP_057699.2:p.Gly152=
NM_001190997.3:c.203-4628G=	NP_001177926.1:n.203-4628G=