Canonical Allele Identifier: CA380124632

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282458A>T (hg19) ; chr11:g.35260911A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260911A>T , CM000673.2:g.35260911A>T	GRCh38
NC_000011.9:g.35282458A>T , CM000673.1:g.35282458A>T	GRCh37
NC_000011.8:g.35239034A>T	NCBI36
NG_008727.1:g.163648T>A
NG_008727.2:g.163648T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1708T>A MANE Select	ENSP00000278379.3:p.Trp570Arg
ENST00000395750.6:c.1696T>A	ENSP00000379099.2:p.Trp566Arg
ENST00000395753.6:c.1681T>A	ENSP00000379102.1:p.Trp561Arg
ENST00000479543.2:n.1260T>A
ENST00000642171.1:c.*90T>A	ENSP00000495538.1:n.*90T>A
ENST00000642448.1:n.1800T>A
ENST00000642769.1:c.974T>A
ENST00000643000.1:c.1681T>A	ENSP00000495164.1:p.Trp561Arg
ENST00000643134.1:c.1695T>A	ENSP00000495188.1:p.Leu565=
ENST00000643522.1:c.1474T>A	ENSP00000496375.1:p.Trp492Arg
ENST00000644050.1:c.1681T>A	ENSP00000496123.1:p.Trp561Arg
ENST00000644299.1:c.1681T>A	ENSP00000494669.1:p.Trp561Arg
ENST00000644459.1:c.*200T>A	ENSP00000495861.1:n.*200T>A
ENST00000644779.1:c.1819T>A	ENSP00000494258.1:p.Trp607Arg
ENST00000644868.1:c.1770T>A	ENSP00000496760.1:n.1770T>A
ENST00000645194.1:c.1681T>A	ENSP00000496093.1:p.Trp561Arg
ENST00000645303.1:c.1723T>A	ENSP00000496667.1:p.Trp575Arg
ENST00000645542.1:n.414T>A
ENST00000645634.1:c.1681T>A	ENSP00000493945.1:p.Trp561Arg
ENST00000646080.1:c.1699T>A	ENSP00000494113.1:p.Trp567Arg
ENST00000647076.1:c.449T>A
ENST00000647104.1:c.1681T>A	ENSP00000494025.1:p.Trp561Arg
ENST00000278379.7:c.1708T>A	ENSP00000278379.3:p.Trp570Arg
ENST00000395750.5:c.1681T>A	ENSP00000379099.1:p.Trp561Arg
ENST00000395753.5:c.1681T>A	ENSP00000379102.1:p.Trp561Arg
ENST00000464522.2:c.219+4616T>A	ENSP00000435406.1:n.219+4616T>A
ENST00000479543.1:n.524T>A
NM_001195728.2:c.1681T>A	NP_001182657.1:p.Trp561Arg
NM_001252652.1:c.1681T>A	NP_001239581.1:p.Trp561Arg
NM_004171.3:c.1708T>A	NP_004162.2:p.Trp570Arg
XM_005253067.1:c.1699T>A	XP_005253124.1:p.Trp567Arg
XM_011520284.1:c.1756T>A	XP_011518586.1:p.Trp586Arg
XM_011520285.1:c.1696T>A	XP_011518587.1:p.Trp566Arg
XM_011520286.1:c.1621T>A	XP_011518588.1:p.Trp541Arg
XM_011520287.1:c.1522T>A	XP_011518589.1:p.Trp508Arg
XM_011520285.2:c.1696T>A	XP_011518587.1:p.Trp566Arg
XM_017018136.1:c.1723T>A	XP_016873625.1:p.Trp575Arg
XM_017018137.1:c.1681T>A	XP_016873626.1:p.Trp561Arg
XM_017018138.1:c.1681T>A	XP_016873627.1:p.Trp561Arg
XM_017018139.1:c.1474T>A	XP_016873628.1:p.Trp492Arg
NM_004171.4:c.1708T>A MANE Select	NP_004162.2:p.Trp570Arg
NM_001195728.3:c.1681T>A	NP_001182657.1:p.Trp561Arg
NM_001252652.2:c.1681T>A	NP_001239581.1:p.Trp561Arg