Canonical Allele Identifier: CA380124682

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282468C>A (hg19) ; chr11:g.35260921C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260921C>A , CM000673.2:g.35260921C>A	GRCh38
NC_000011.9:g.35282468C>A , CM000673.1:g.35282468C>A	GRCh37
NC_000011.8:g.35239044C>A	NCBI36
NG_008727.1:g.163638G>T
NG_008727.2:g.163638G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1698G>T MANE Select	ENSP00000278379.3:p.Glu566Asp
ENST00000395750.6:c.1686G>T	ENSP00000379099.2:p.Glu562Asp
ENST00000395753.6:c.1671G>T	ENSP00000379102.1:p.Glu557Asp
ENST00000479543.2:n.1250G>T
ENST00000642171.1:c.*80G>T	ENSP00000495538.1:n.*80G>T
ENST00000642448.1:n.1790G>T
ENST00000642769.1:c.964G>T
ENST00000643000.1:c.1671G>T	ENSP00000495164.1:p.Glu557Asp
ENST00000643134.1:c.1685G>T	ENSP00000495188.1:p.Arg562Met
ENST00000643522.1:c.1464G>T	ENSP00000496375.1:p.Glu488Asp
ENST00000644050.1:c.1671G>T	ENSP00000496123.1:p.Glu557Asp
ENST00000644299.1:c.1671G>T	ENSP00000494669.1:p.Glu557Asp
ENST00000644459.1:c.*190G>T	ENSP00000495861.1:n.*190G>T
ENST00000644779.1:c.1809G>T	ENSP00000494258.1:p.Glu603Asp
ENST00000644868.1:c.1760G>T	ENSP00000496760.1:n.1760G>T
ENST00000645194.1:c.1671G>T	ENSP00000496093.1:p.Glu557Asp
ENST00000645303.1:c.1713G>T	ENSP00000496667.1:p.Glu571Asp
ENST00000645542.1:n.404G>T
ENST00000645634.1:c.1671G>T	ENSP00000493945.1:p.Glu557Asp
ENST00000646080.1:c.1689G>T	ENSP00000494113.1:p.Glu563Asp
ENST00000647076.1:c.439G>T
ENST00000647104.1:c.1671G>T	ENSP00000494025.1:p.Glu557Asp
ENST00000278379.7:c.1698G>T	ENSP00000278379.3:p.Glu566Asp
ENST00000395750.5:c.1671G>T	ENSP00000379099.1:p.Glu557Asp
ENST00000395753.5:c.1671G>T	ENSP00000379102.1:p.Glu557Asp
ENST00000464522.2:c.219+4606G>T	ENSP00000435406.1:n.219+4606G>T
ENST00000479543.1:n.514G>T
NM_001195728.2:c.1671G>T	NP_001182657.1:p.Glu557Asp
NM_001252652.1:c.1671G>T	NP_001239581.1:p.Glu557Asp
NM_004171.3:c.1698G>T	NP_004162.2:p.Glu566Asp
XM_005253067.1:c.1689G>T	XP_005253124.1:p.Glu563Asp
XM_011520284.1:c.1746G>T	XP_011518586.1:p.Glu582Asp
XM_011520285.1:c.1686G>T	XP_011518587.1:p.Glu562Asp
XM_011520286.1:c.1611G>T	XP_011518588.1:p.Glu537Asp
XM_011520287.1:c.1512G>T	XP_011518589.1:p.Glu504Asp
XM_011520285.2:c.1686G>T	XP_011518587.1:p.Glu562Asp
XM_017018136.1:c.1713G>T	XP_016873625.1:p.Glu571Asp
XM_017018137.1:c.1671G>T	XP_016873626.1:p.Glu557Asp
XM_017018138.1:c.1671G>T	XP_016873627.1:p.Glu557Asp
XM_017018139.1:c.1464G>T	XP_016873628.1:p.Glu488Asp
NM_004171.4:c.1698G>T MANE Select	NP_004162.2:p.Glu566Asp
NM_001195728.3:c.1671G>T	NP_001182657.1:p.Glu557Asp
NM_001252652.2:c.1671G>T	NP_001239581.1:p.Glu557Asp