Canonical Allele Identifier: CA383602775

Gene: SLC6A13

Linked Data

• MyVariant Identifiers: chr12:g.351797T>C (hg19) ; chr12:g.242631T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.242631T>C , CM000674.2:g.242631T>C	GRCh38
NC_000012.11:g.351797T>C , CM000674.1:g.351797T>C	GRCh37
NC_000012.10:g.222058T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343164.9:c.461A>G MANE Select	ENSP00000339260.4:p.Tyr154Cys
ENST00000343164.8:c.461A>G	ENSP00000339260.4:p.Tyr154Cys
ENST00000445055.6:c.203-4621A>G	ENSP00000407104.2:n.203-4621A>G
ENST00000536842.5:n.514A>G
ENST00000539260.1:c.*100A>G	ENSP00000437386.1:n.*100A>G
ENST00000542272.5:c.104A>G	ENSP00000443466.1:p.Tyr35Cys
ENST00000546319.5:c.203-4621A>G	ENSP00000444606.1:n.203-4621A>G
NM_001190997.2:c.203-4621A>G	NP_001177926.1:n.203-4621A>G
NM_016615.4:c.461A>G	NP_057699.2:p.Tyr154Cys
XM_005253749.2:c.527A>G	XP_005253806.1:p.Tyr176Cys
XM_011521012.1:c.104A>G	XP_011519314.1:p.Tyr35Cys
XM_011521013.1:c.-199A>G	XP_011519315.1:n.-199A>G
XM_011521014.1:c.-199A>G	XP_011519316.1:n.-199A>G
XM_011521012.2:c.104A>G	XP_011519314.1:p.Tyr35Cys
XM_017019844.1:c.461A>G	XP_016875333.1:p.Tyr154Cys
XM_017019846.1:c.461A>G	XP_016875335.1:p.Tyr154Cys
XM_017019847.1:c.461A>G	XP_016875336.1:p.Tyr154Cys
XR_001748849.1:n.514A>G
XR_002957372.1:n.514A>G
NM_016615.5:c.461A>G MANE Select	NP_057699.2:p.Tyr154Cys
NM_001190997.3:c.203-4621A>G	NP_001177926.1:n.203-4621A>G