Canonical Allele Identifier: CA383602743

Gene: SLC6A13

Linked Data

• MyVariant Identifiers: chr12:g.351791T>G (hg19) ; chr12:g.242625T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.242625T>G , CM000674.2:g.242625T>G	GRCh38
NC_000012.11:g.351791T>G , CM000674.1:g.351791T>G	GRCh37
NC_000012.10:g.222052T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343164.9:c.467A>C MANE Select	ENSP00000339260.4:p.Glu156Ala
ENST00000343164.8:c.467A>C	ENSP00000339260.4:p.Glu156Ala
ENST00000445055.6:c.203-4615A>C	ENSP00000407104.2:n.203-4615A>C
ENST00000536842.5:n.520A>C
ENST00000539260.1:c.*106A>C	ENSP00000437386.1:n.*106A>C
ENST00000542272.5:c.110A>C	ENSP00000443466.1:p.Glu37Ala
ENST00000546319.5:c.203-4615A>C	ENSP00000444606.1:n.203-4615A>C
NM_001190997.2:c.203-4615A>C	NP_001177926.1:n.203-4615A>C
NM_016615.4:c.467A>C	NP_057699.2:p.Glu156Ala
XM_005253749.2:c.533A>C	XP_005253806.1:p.Glu178Ala
XM_011521012.1:c.110A>C	XP_011519314.1:p.Glu37Ala
XM_011521013.1:c.-193A>C	XP_011519315.1:n.-193A>C
XM_011521014.1:c.-193A>C	XP_011519316.1:n.-193A>C
XM_011521012.2:c.110A>C	XP_011519314.1:p.Glu37Ala
XM_017019844.1:c.467A>C	XP_016875333.1:p.Glu156Ala
XM_017019846.1:c.467A>C	XP_016875335.1:p.Glu156Ala
XM_017019847.1:c.467A>C	XP_016875336.1:p.Glu156Ala
XR_001748849.1:n.520A>C
XR_002957372.1:n.520A>C
NM_016615.5:c.467A>C MANE Select	NP_057699.2:p.Glu156Ala
NM_001190997.3:c.203-4615A>C	NP_001177926.1:n.203-4615A>C