Canonical Allele Identifier: CA1963611193
Gene: SLC1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35261215C= , CM000673.2:g.35261215C= GRCh38
NC_000011.9:g.35282762C= , CM000673.1:g.35282762C= GRCh37
NC_000011.8:g.35239338C= NCBI36
NG_008727.1:g.163344G=
NG_008727.2:g.163344G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278379.9:c.1654-250G= MANE Select ENSP00000278379.3:n.1654-250G=
ENST00000395750.6:c.1642-250G= ENSP00000379099.2:n.1642-250G=
ENST00000395753.6:c.1627-250G= ENSP00000379102.1:n.1627-250G=
ENST00000479543.2:n.1206-250G=
ENST00000642171.1:c.*36-250G= ENSP00000495538.1:n.*36-250G=
ENST00000642448.1:n.1746-250G=
ENST00000642769.1:c.920-250G=
ENST00000643000.1:c.1627-250G= ENSP00000495164.1:n.1627-250G=
ENST00000643134.1:c.1654-263G= ENSP00000495188.1:n.1654-263G=
ENST00000643522.1:c.1420-250G= ENSP00000496375.1:n.1420-250G=
ENST00000644050.1:c.1627-250G= ENSP00000496123.1:n.1627-250G=
ENST00000644299.1:c.1627-250G= ENSP00000494669.1:n.1627-250G=
ENST00000644459.1:c.*146-250G= ENSP00000495861.1:n.*146-250G=
ENST00000644779.1:c.1765-250G= ENSP00000494258.1:n.1765-250G=
ENST00000644868.1:c.1716-250G= ENSP00000496760.1:n.1716-250G=
ENST00000645194.1:c.1627-250G= ENSP00000496093.1:n.1627-250G=
ENST00000645303.1:c.1669-250G= ENSP00000496667.1:n.1669-250G=
ENST00000645542.1:n.360-250G=
ENST00000645634.1:c.1627-250G= ENSP00000493945.1:n.1627-250G=
ENST00000646080.1:c.1645-250G= ENSP00000494113.1:n.1645-250G=
ENST00000647076.1:c.395-250G=
ENST00000647104.1:c.1627-250G= ENSP00000494025.1:n.1627-250G=
ENST00000278379.7:c.1654-250G= ENSP00000278379.3:n.1654-250G=
ENST00000395750.5:c.1627-250G= ENSP00000379099.1:n.1627-250G=
ENST00000395753.5:c.1627-250G= ENSP00000379102.1:n.1627-250G=
ENST00000464522.2:c.219+4312G= ENSP00000435406.1:n.219+4312G=
ENST00000479543.1:n.470-250G=
NM_001195728.2:c.1627-250G= NP_001182657.1:n.1627-250G=
NM_001252652.1:c.1627-250G= NP_001239581.1:n.1627-250G=
NM_004171.3:c.1654-250G= NP_004162.2:n.1654-250G=
XM_005253067.1:c.1645-250G= XP_005253124.1:n.1645-250G=
XM_011520284.1:c.1702-250G= XP_011518586.1:n.1702-250G=
XM_011520285.1:c.1642-250G= XP_011518587.1:n.1642-250G=
XM_011520286.1:c.1567-250G= XP_011518588.1:n.1567-250G=
XM_011520287.1:c.1468-250G= XP_011518589.1:n.1468-250G=
XM_011520285.2:c.1642-250G= XP_011518587.1:n.1642-250G=
XM_017018136.1:c.1669-250G= XP_016873625.1:n.1669-250G=
XM_017018137.1:c.1627-250G= XP_016873626.1:n.1627-250G=
XM_017018138.1:c.1627-250G= XP_016873627.1:n.1627-250G=
XM_017018139.1:c.1420-250G= XP_016873628.1:n.1420-250G=
NM_004171.4:c.1654-250G= MANE Select NP_004162.2:n.1654-250G=
NM_001195728.3:c.1627-250G= NP_001182657.1:n.1627-250G=
NM_001252652.2:c.1627-250G= NP_001239581.1:n.1627-250G=