Canonical Allele Identifier: CA380124665

Gene: SLC1A2

Linked Data

• MyVariant Identifiers: chr11:g.35282466T>C (hg19) ; chr11:g.35260919T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.35260919T>C , CM000673.2:g.35260919T>C	GRCh38
NC_000011.9:g.35282466T>C , CM000673.1:g.35282466T>C	GRCh37
NC_000011.8:g.35239042T>C	NCBI36
NG_008727.1:g.163640A>G
NG_008727.2:g.163640A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278379.9:c.1700A>G MANE Select	ENSP00000278379.3:p.Glu567Gly
ENST00000395750.6:c.1688A>G	ENSP00000379099.2:p.Glu563Gly
ENST00000395753.6:c.1673A>G	ENSP00000379102.1:p.Glu558Gly
ENST00000479543.2:n.1252A>G
ENST00000642171.1:c.*82A>G	ENSP00000495538.1:n.*82A>G
ENST00000642448.1:n.1792A>G
ENST00000642769.1:c.966A>G
ENST00000643000.1:c.1673A>G	ENSP00000495164.1:p.Glu558Gly
ENST00000643134.1:c.1687A>G	ENSP00000495188.1:p.Lys563Glu
ENST00000643522.1:c.1466A>G	ENSP00000496375.1:p.Glu489Gly
ENST00000644050.1:c.1673A>G	ENSP00000496123.1:p.Glu558Gly
ENST00000644299.1:c.1673A>G	ENSP00000494669.1:p.Glu558Gly
ENST00000644459.1:c.*192A>G	ENSP00000495861.1:n.*192A>G
ENST00000644779.1:c.1811A>G	ENSP00000494258.1:p.Glu604Gly
ENST00000644868.1:c.1762A>G	ENSP00000496760.1:n.1762A>G
ENST00000645194.1:c.1673A>G	ENSP00000496093.1:p.Glu558Gly
ENST00000645303.1:c.1715A>G	ENSP00000496667.1:p.Glu572Gly
ENST00000645542.1:n.406A>G
ENST00000645634.1:c.1673A>G	ENSP00000493945.1:p.Glu558Gly
ENST00000646080.1:c.1691A>G	ENSP00000494113.1:p.Glu564Gly
ENST00000647076.1:c.441A>G
ENST00000647104.1:c.1673A>G	ENSP00000494025.1:p.Glu558Gly
ENST00000278379.7:c.1700A>G	ENSP00000278379.3:p.Glu567Gly
ENST00000395750.5:c.1673A>G	ENSP00000379099.1:p.Glu558Gly
ENST00000395753.5:c.1673A>G	ENSP00000379102.1:p.Glu558Gly
ENST00000464522.2:c.219+4608A>G	ENSP00000435406.1:n.219+4608A>G
ENST00000479543.1:n.516A>G
NM_001195728.2:c.1673A>G	NP_001182657.1:p.Glu558Gly
NM_001252652.1:c.1673A>G	NP_001239581.1:p.Glu558Gly
NM_004171.3:c.1700A>G	NP_004162.2:p.Glu567Gly
XM_005253067.1:c.1691A>G	XP_005253124.1:p.Glu564Gly
XM_011520284.1:c.1748A>G	XP_011518586.1:p.Glu583Gly
XM_011520285.1:c.1688A>G	XP_011518587.1:p.Glu563Gly
XM_011520286.1:c.1613A>G	XP_011518588.1:p.Glu538Gly
XM_011520287.1:c.1514A>G	XP_011518589.1:p.Glu505Gly
XM_011520285.2:c.1688A>G	XP_011518587.1:p.Glu563Gly
XM_017018136.1:c.1715A>G	XP_016873625.1:p.Glu572Gly
XM_017018137.1:c.1673A>G	XP_016873626.1:p.Glu558Gly
XM_017018138.1:c.1673A>G	XP_016873627.1:p.Glu558Gly
XM_017018139.1:c.1466A>G	XP_016873628.1:p.Glu489Gly
NM_004171.4:c.1700A>G MANE Select	NP_004162.2:p.Glu567Gly
NM_001195728.3:c.1673A>G	NP_001182657.1:p.Glu558Gly
NM_001252652.2:c.1673A>G	NP_001239581.1:p.Glu558Gly