Canonical Allele Identifier: CA1963610841
Gene: SLC1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35260899T= , CM000673.2:g.35260899T= GRCh38
NC_000011.9:g.35282446T= , CM000673.1:g.35282446T= GRCh37
NC_000011.8:g.35239022T= NCBI36
NG_008727.1:g.163660A=
NG_008727.2:g.163660A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278379.9:c.1720A= MANE Select ENSP00000278379.3:p.Lys574=
ENST00000395750.6:c.1708A= ENSP00000379099.2:p.Lys570=
ENST00000395753.6:c.1693A= ENSP00000379102.1:p.Lys565=
ENST00000479543.2:n.1272A=
ENST00000642171.1:c.*102A= ENSP00000495538.1:n.*102A=
ENST00000642448.1:n.1812A=
ENST00000642769.1:c.986A=
ENST00000643000.1:c.1693A= ENSP00000495164.1:p.Lys565=
ENST00000643134.1:c.1707A= ENSP00000495188.1:p.Arg569=
ENST00000643522.1:c.1486A= ENSP00000496375.1:p.Lys496=
ENST00000644050.1:c.1693A= ENSP00000496123.1:p.Lys565=
ENST00000644299.1:c.1693A= ENSP00000494669.1:p.Lys565=
ENST00000644459.1:c.*212A= ENSP00000495861.1:n.*212A=
ENST00000644779.1:c.1831A= ENSP00000494258.1:p.Lys611=
ENST00000644868.1:c.1782A= ENSP00000496760.1:n.1782A=
ENST00000645194.1:c.1693A= ENSP00000496093.1:p.Lys565=
ENST00000645303.1:c.1735A= ENSP00000496667.1:p.Lys579=
ENST00000645542.1:n.426A=
ENST00000645634.1:c.1693A= ENSP00000493945.1:p.Lys565=
ENST00000646080.1:c.1711A= ENSP00000494113.1:p.Lys571=
ENST00000647076.1:c.461A=
ENST00000647104.1:c.1693A= ENSP00000494025.1:p.Lys565=
ENST00000278379.7:c.1720A= ENSP00000278379.3:p.Lys574=
ENST00000395750.5:c.1693A= ENSP00000379099.1:p.Lys565=
ENST00000395753.5:c.1693A= ENSP00000379102.1:p.Lys565=
ENST00000464522.2:c.219+4628A= ENSP00000435406.1:n.219+4628A=
ENST00000479543.1:n.536A=
NM_001195728.2:c.1693A= NP_001182657.1:p.Lys565=
NM_001252652.1:c.1693A= NP_001239581.1:p.Lys565=
NM_004171.3:c.1720A= NP_004162.2:p.Lys574=
XM_005253067.1:c.1711A= XP_005253124.1:p.Lys571=
XM_011520284.1:c.1768A= XP_011518586.1:p.Lys590=
XM_011520285.1:c.1708A= XP_011518587.1:p.Lys570=
XM_011520286.1:c.1633A= XP_011518588.1:p.Lys545=
XM_011520287.1:c.1534A= XP_011518589.1:p.Lys512=
XM_011520285.2:c.1708A= XP_011518587.1:p.Lys570=
XM_017018136.1:c.1735A= XP_016873625.1:p.Lys579=
XM_017018137.1:c.1693A= XP_016873626.1:p.Lys565=
XM_017018138.1:c.1693A= XP_016873627.1:p.Lys565=
XM_017018139.1:c.1486A= XP_016873628.1:p.Lys496=
NM_004171.4:c.1720A= MANE Select NP_004162.2:p.Lys574=
NM_001195728.3:c.1693A= NP_001182657.1:p.Lys565=
NM_001252652.2:c.1693A= NP_001239581.1:p.Lys565=