Canonical Allele Identifier: CA1963610773
Gene: SLC1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.35260836_35260837delinsTC , CM000673.2:g.35260836_35260837delinsTC GRCh38
NC_000011.9:g.35282383_35282384delinsTC , CM000673.1:g.35282383_35282384delinsTC GRCh37
NC_000011.8:g.35238959_35238960delinsTC NCBI36
NG_008727.1:g.163722_163723delinsGA
NG_008727.2:g.163722_163723delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000278379.9:c.*57_*58delinsGA MANE Select ENSP00000278379.3:n.*57_*58delinsGA
ENST00000395750.6:c.*57_*58delinsGA ENSP00000379099.2:n.*57_*58delinsGA
ENST00000395753.6:c.*57_*58delinsGA ENSP00000379102.1:n.*57_*58delinsGA
ENST00000479543.2:n.1334_1335delinsGA
ENST00000642171.1:c.*164_*165delinsGA ENSP00000495538.1:n.*164_*165delinsGA
ENST00000642448.1:n.1874_1875delinsGA
ENST00000642769.1:c.1041+7_1041+8delinsGA
ENST00000643000.1:c.*57_*58delinsGA ENSP00000495164.1:n.*57_*58delinsGA
ENST00000643522.1:c.*57_*58delinsGA ENSP00000496375.1:n.*57_*58delinsGA
ENST00000644050.1:c.*57_*58delinsGA ENSP00000496123.1:n.*57_*58delinsGA
ENST00000644299.1:c.*57_*58delinsGA ENSP00000494669.1:n.*57_*58delinsGA
ENST00000644459.1:c.*274_*275delinsGA ENSP00000495861.1:n.*274_*275delinsGA
ENST00000644779.1:c.*57_*58delinsGA ENSP00000494258.1:n.*57_*58delinsGA
ENST00000644868.1:c.1844_1845delinsGA ENSP00000496760.1:n.1844_1845delinsGA
ENST00000645194.1:c.*57_*58delinsGA ENSP00000496093.1:n.*57_*58delinsGA
ENST00000645303.1:c.*57_*58delinsGA ENSP00000496667.1:n.*57_*58delinsGA
ENST00000645542.1:n.488_489delinsGA
ENST00000645634.1:c.*57_*58delinsGA ENSP00000493945.1:n.*57_*58delinsGA
ENST00000646080.1:c.*57_*58delinsGA ENSP00000494113.1:n.*57_*58delinsGA
ENST00000647076.1:c.516+7_516+8delinsGA
ENST00000647104.1:c.*57_*58delinsGA ENSP00000494025.1:n.*57_*58delinsGA
ENST00000278379.7:c.*57_*58delinsGA ENSP00000278379.3:n.*57_*58delinsGA
ENST00000395750.5:c.*57_*58delinsGA ENSP00000379099.1:n.*57_*58delinsGA
ENST00000395753.5:c.*57_*58delinsGA ENSP00000379102.1:n.*57_*58delinsGA
ENST00000464522.2:c.219+4690_219+4691delinsGA ENSP00000435406.1:n.219+4690_219+4691delinsGA
NM_001195728.2:c.*57_*58delinsGA NP_001182657.1:n.*57_*58delinsGA
NM_001252652.1:c.*57_*58delinsGA NP_001239581.1:n.*57_*58delinsGA
NM_004171.3:c.*57_*58delinsGA NP_004162.2:n.*57_*58delinsGA
XM_005253067.1:c.*57_*58delinsGA XP_005253124.1:n.*57_*58delinsGA
XM_011520284.1:c.*57_*58delinsGA XP_011518586.1:n.*57_*58delinsGA
XM_011520285.1:c.*57_*58delinsGA XP_011518587.1:n.*57_*58delinsGA
XM_011520286.1:c.*57_*58delinsGA XP_011518588.1:n.*57_*58delinsGA
XM_011520287.1:c.*57_*58delinsGA XP_011518589.1:n.*57_*58delinsGA
XM_011520285.2:c.*57_*58delinsGA XP_011518587.1:n.*57_*58delinsGA
XM_017018136.1:c.*57_*58delinsGA XP_016873625.1:n.*57_*58delinsGA
XM_017018137.1:c.*57_*58delinsGA XP_016873626.1:n.*57_*58delinsGA
XM_017018138.1:c.*57_*58delinsGA XP_016873627.1:n.*57_*58delinsGA
XM_017018139.1:c.*57_*58delinsGA XP_016873628.1:n.*57_*58delinsGA
NM_004171.4:c.*57_*58delinsGA MANE Select NP_004162.2:n.*57_*58delinsGA
NM_001195728.3:c.*57_*58delinsGA NP_001182657.1:n.*57_*58delinsGA
NM_001252652.2:c.*57_*58delinsGA NP_001239581.1:n.*57_*58delinsGA