Canonical Allele Identifier: CA1963610927
Gene: SLC1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35260936G= , CM000673.2:g.35260936G= GRCh38
NC_000011.9:g.35282483G= , CM000673.1:g.35282483G= GRCh37
NC_000011.8:g.35239059G= NCBI36
NG_008727.1:g.163623C=
NG_008727.2:g.163623C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278379.9:c.1683C= MANE Select ENSP00000278379.3:p.Ala561=
ENST00000395750.6:c.1671C= ENSP00000379099.2:p.Ala557=
ENST00000395753.6:c.1656C= ENSP00000379102.1:p.Ala552=
ENST00000479543.2:n.1235C=
ENST00000642171.1:c.*65C= ENSP00000495538.1:n.*65C=
ENST00000642448.1:n.1775C=
ENST00000642769.1:c.949C=
ENST00000643000.1:c.1656C= ENSP00000495164.1:p.Ala552=
ENST00000643134.1:c.1670C= ENSP00000495188.1:p.Pro557=
ENST00000643522.1:c.1449C= ENSP00000496375.1:p.Ala483=
ENST00000644050.1:c.1656C= ENSP00000496123.1:p.Ala552=
ENST00000644299.1:c.1656C= ENSP00000494669.1:p.Ala552=
ENST00000644459.1:c.*175C= ENSP00000495861.1:n.*175C=
ENST00000644779.1:c.1794C= ENSP00000494258.1:p.Ala598=
ENST00000644868.1:c.1745C= ENSP00000496760.1:n.1745C=
ENST00000645194.1:c.1656C= ENSP00000496093.1:p.Ala552=
ENST00000645303.1:c.1698C= ENSP00000496667.1:p.Ala566=
ENST00000645542.1:n.389C=
ENST00000645634.1:c.1656C= ENSP00000493945.1:p.Ala552=
ENST00000646080.1:c.1674C= ENSP00000494113.1:p.Ala558=
ENST00000647076.1:c.424C=
ENST00000647104.1:c.1656C= ENSP00000494025.1:p.Ala552=
ENST00000278379.7:c.1683C= ENSP00000278379.3:p.Ala561=
ENST00000395750.5:c.1656C= ENSP00000379099.1:p.Ala552=
ENST00000395753.5:c.1656C= ENSP00000379102.1:p.Ala552=
ENST00000464522.2:c.219+4591C= ENSP00000435406.1:n.219+4591C=
ENST00000479543.1:n.499C=
NM_001195728.2:c.1656C= NP_001182657.1:p.Ala552=
NM_001252652.1:c.1656C= NP_001239581.1:p.Ala552=
NM_004171.3:c.1683C= NP_004162.2:p.Ala561=
XM_005253067.1:c.1674C= XP_005253124.1:p.Ala558=
XM_011520284.1:c.1731C= XP_011518586.1:p.Ala577=
XM_011520285.1:c.1671C= XP_011518587.1:p.Ala557=
XM_011520286.1:c.1596C= XP_011518588.1:p.Ala532=
XM_011520287.1:c.1497C= XP_011518589.1:p.Ala499=
XM_011520285.2:c.1671C= XP_011518587.1:p.Ala557=
XM_017018136.1:c.1698C= XP_016873625.1:p.Ala566=
XM_017018137.1:c.1656C= XP_016873626.1:p.Ala552=
XM_017018138.1:c.1656C= XP_016873627.1:p.Ala552=
XM_017018139.1:c.1449C= XP_016873628.1:p.Ala483=
NM_004171.4:c.1683C= MANE Select NP_004162.2:p.Ala561=
NM_001195728.3:c.1656C= NP_001182657.1:p.Ala552=
NM_001252652.2:c.1656C= NP_001239581.1:p.Ala552=