Canonical Allele Identifier: CA2011406991

Gene: SLC6A13

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.240132C= , CM000674.2:g.240132C=	GRCh38
NC_000012.11:g.349298C= , CM000674.1:g.349298C=	GRCh37
NC_000012.10:g.219559C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343164.9:c.479-2122G= MANE Select	ENSP00000339260.4:n.479-2122G=
ENST00000343164.8:c.479-2122G=	ENSP00000339260.4:n.479-2122G=
ENST00000445055.6:c.203-2122G=	ENSP00000407104.2:n.203-2122G=
ENST00000536842.5:n.532-2122G=
ENST00000539260.1:c.*118-2122G=	ENSP00000437386.1:n.*118-2122G=
ENST00000542272.5:c.122-1789G=	ENSP00000443466.1:n.122-1789G=
ENST00000546319.5:c.203-2122G=	ENSP00000444606.1:n.203-2122G=
NM_001190997.2:c.203-2122G=	NP_001177926.1:n.203-2122G=
NM_016615.4:c.479-2122G=	NP_057699.2:n.479-2122G=
XM_005253749.2:c.545-2122G=	XP_005253806.1:n.545-2122G=
XM_011521012.1:c.122-2122G=	XP_011519314.1:n.122-2122G=
XM_011521013.1:c.-181-1789G=	XP_011519315.1:n.-181-1789G=
XM_011521014.1:c.-181-1789G=	XP_011519316.1:n.-181-1789G=
XM_011521012.2:c.122-2122G=	XP_011519314.1:n.122-2122G=
XM_017019844.1:c.479-2122G=	XP_016875333.1:n.479-2122G=
XM_017019846.1:c.479-2122G=	XP_016875335.1:n.479-2122G=
XM_017019847.1:c.479-2122G=	XP_016875336.1:n.479-2122G=
XR_001748849.1:n.532-2122G=
XR_002957372.1:n.532-2122G=
NM_016615.5:c.479-2122G= MANE Select	NP_057699.2:n.479-2122G=
NM_001190997.3:c.203-2122G=	NP_001177926.1:n.203-2122G=