Canonical Allele Identifier: CA380124821

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282508G>A (hg19) ; chr11:g.35260961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260961G>A , CM000673.2:g.35260961G>A	GRCh38
NC_000011.9:g.35282508G>A , CM000673.1:g.35282508G>A	GRCh37
NC_000011.8:g.35239084G>A	NCBI36
NG_008727.1:g.163598C>T
NG_008727.2:g.163598C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1658C>T MANE Select	ENSP00000278379.3:p.Thr553Ile
ENST00000395750.6:c.1646C>T	ENSP00000379099.2:p.Thr549Ile
ENST00000395753.6:c.1631C>T	ENSP00000379102.1:p.Thr544Ile
ENST00000479543.2:n.1210C>T
ENST00000642171.1:c.*40C>T	ENSP00000495538.1:n.*40C>T
ENST00000642448.1:n.1750C>T
ENST00000642769.1:c.924C>T
ENST00000643000.1:c.1631C>T	ENSP00000495164.1:p.Thr544Ile
ENST00000643134.1:c.1654-9C>T	ENSP00000495188.1:n.1654-9C>T
ENST00000643522.1:c.1424C>T	ENSP00000496375.1:p.Thr475Ile
ENST00000644050.1:c.1631C>T	ENSP00000496123.1:p.Thr544Ile
ENST00000644299.1:c.1631C>T	ENSP00000494669.1:p.Thr544Ile
ENST00000644459.1:c.*150C>T	ENSP00000495861.1:n.*150C>T
ENST00000644779.1:c.1769C>T	ENSP00000494258.1:p.Thr590Ile
ENST00000644868.1:c.1720C>T	ENSP00000496760.1:n.1720C>T
ENST00000645194.1:c.1631C>T	ENSP00000496093.1:p.Thr544Ile
ENST00000645303.1:c.1673C>T	ENSP00000496667.1:p.Thr558Ile
ENST00000645542.1:n.364C>T
ENST00000645634.1:c.1631C>T	ENSP00000493945.1:p.Thr544Ile
ENST00000646080.1:c.1649C>T	ENSP00000494113.1:p.Thr550Ile
ENST00000647076.1:c.399C>T
ENST00000647104.1:c.1631C>T	ENSP00000494025.1:p.Thr544Ile
ENST00000278379.7:c.1658C>T	ENSP00000278379.3:p.Thr553Ile
ENST00000395750.5:c.1631C>T	ENSP00000379099.1:p.Thr544Ile
ENST00000395753.5:c.1631C>T	ENSP00000379102.1:p.Thr544Ile
ENST00000464522.2:c.219+4566C>T	ENSP00000435406.1:n.219+4566C>T
ENST00000479543.1:n.474C>T
NM_001195728.2:c.1631C>T	NP_001182657.1:p.Thr544Ile
NM_001252652.1:c.1631C>T	NP_001239581.1:p.Thr544Ile
NM_004171.3:c.1658C>T	NP_004162.2:p.Thr553Ile
XM_005253067.1:c.1649C>T	XP_005253124.1:p.Thr550Ile
XM_011520284.1:c.1706C>T	XP_011518586.1:p.Thr569Ile
XM_011520285.1:c.1646C>T	XP_011518587.1:p.Thr549Ile
XM_011520286.1:c.1571C>T	XP_011518588.1:p.Thr524Ile
XM_011520287.1:c.1472C>T	XP_011518589.1:p.Thr491Ile
XM_011520285.2:c.1646C>T	XP_011518587.1:p.Thr549Ile
XM_017018136.1:c.1673C>T	XP_016873625.1:p.Thr558Ile
XM_017018137.1:c.1631C>T	XP_016873626.1:p.Thr544Ile
XM_017018138.1:c.1631C>T	XP_016873627.1:p.Thr544Ile
XM_017018139.1:c.1424C>T	XP_016873628.1:p.Thr475Ile
NM_004171.4:c.1658C>T MANE Select	NP_004162.2:p.Thr553Ile
NM_001195728.3:c.1631C>T	NP_001182657.1:p.Thr544Ile
NM_001252652.2:c.1631C>T	NP_001239581.1:p.Thr544Ile