Canonical Allele Identifier: CA383602700

Gene: SLC6A13

Linked Data

• MyVariant Identifiers: chr12:g.351783T>C (hg19) ; chr12:g.242617T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.242617T>C , CM000674.2:g.242617T>C	GRCh38
NC_000012.11:g.351783T>C , CM000674.1:g.351783T>C	GRCh37
NC_000012.10:g.222044T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343164.9:c.475A>G MANE Select	ENSP00000339260.4:p.Thr159Ala
ENST00000343164.8:c.475A>G	ENSP00000339260.4:p.Thr159Ala
ENST00000445055.6:c.203-4607A>G	ENSP00000407104.2:n.203-4607A>G
ENST00000536842.5:n.528A>G
ENST00000539260.1:c.*114A>G	ENSP00000437386.1:n.*114A>G
ENST00000542272.5:c.118A>G	ENSP00000443466.1:p.Thr40Ala
ENST00000546319.5:c.203-4607A>G	ENSP00000444606.1:n.203-4607A>G
NM_001190997.2:c.203-4607A>G	NP_001177926.1:n.203-4607A>G
NM_016615.4:c.475A>G	NP_057699.2:p.Thr159Ala
XM_005253749.2:c.541A>G	XP_005253806.1:p.Thr181Ala
XM_011521012.1:c.118A>G	XP_011519314.1:p.Thr40Ala
XM_011521013.1:c.-185A>G	XP_011519315.1:n.-185A>G
XM_011521014.1:c.-185A>G	XP_011519316.1:n.-185A>G
XM_011521012.2:c.118A>G	XP_011519314.1:p.Thr40Ala
XM_017019844.1:c.475A>G	XP_016875333.1:p.Thr159Ala
XM_017019846.1:c.475A>G	XP_016875335.1:p.Thr159Ala
XM_017019847.1:c.475A>G	XP_016875336.1:p.Thr159Ala
XR_001748849.1:n.528A>G
XR_002957372.1:n.528A>G
NM_016615.5:c.475A>G MANE Select	NP_057699.2:p.Thr159Ala
NM_001190997.3:c.203-4607A>G	NP_001177926.1:n.203-4607A>G