Canonical Allele Identifier: CA231381113

Gene: SLC6A13

Linked Data

• dbSNP Id: rs1032568746
• gnomAD v3: 12-242209-C-T
• gnomAD v4: 12-242209-C-T
• MyVariant Identifiers: chr12:g.351375C>T (hg19) ; chr12:g.242209C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.242209C>T , CM000674.2:g.242209C>T	GRCh38
NC_000012.11:g.351375C>T , CM000674.1:g.351375C>T	GRCh37
NC_000012.10:g.221636C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000343164.9:c.478+405G>A MANE Select	ENSP00000339260.4:n.478+405G>A
ENST00000343164.8:c.478+405G>A	ENSP00000339260.4:n.478+405G>A
ENST00000445055.6:c.203-4199G>A	ENSP00000407104.2:n.203-4199G>A
ENST00000536842.5:n.531+405G>A
ENST00000539260.1:c.*117+405G>A	ENSP00000437386.1:n.*117+405G>A
ENST00000542272.5:c.121+405G>A	ENSP00000443466.1:n.121+405G>A
ENST00000546319.5:c.203-4199G>A	ENSP00000444606.1:n.203-4199G>A
NM_001190997.2:c.203-4199G>A	NP_001177926.1:n.203-4199G>A
NM_016615.4:c.478+405G>A	NP_057699.2:n.478+405G>A
XM_005253749.2:c.544+405G>A	XP_005253806.1:n.544+405G>A
XM_011521012.1:c.121+405G>A	XP_011519314.1:n.121+405G>A
XM_011521013.1:c.-182+405G>A	XP_011519315.1:n.-182+405G>A
XM_011521014.1:c.-182+405G>A	XP_011519316.1:n.-182+405G>A
XM_011521012.2:c.121+405G>A	XP_011519314.1:n.121+405G>A
XM_017019844.1:c.478+405G>A	XP_016875333.1:n.478+405G>A
XM_017019846.1:c.478+405G>A	XP_016875335.1:n.478+405G>A
XM_017019847.1:c.478+405G>A	XP_016875336.1:n.478+405G>A
XR_001748849.1:n.531+405G>A
XR_002957372.1:n.531+405G>A
NM_016615.5:c.478+405G>A MANE Select	NP_057699.2:n.478+405G>A
NM_001190997.3:c.203-4199G>A	NP_001177926.1:n.203-4199G>A