Canonical Allele Identifier: CA2646739634
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921817_99921818del , CM000663.2:g.99921817_99921818del GRCh38
NC_000001.10:g.100387373_100387374del , CM000663.1:g.100387373_100387374del GRCh37
NC_000001.9:g.100159961_100159962del NCBI36
NG_012865.1:g.76734_76735del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*166_*167del MANE Select ENSP00000355106.3:n.*166_*167del
ENST00000637337.1:n.4976_4977del
ENST00000294724.8:c.*166_*167del ENSP00000294724.4:n.*166_*167del
ENST00000361302.7:c.*166_*167del ENSP00000354971.3:n.*166_*167del
ENST00000361522.4:c.*166_*167del ENSP00000354635.4:n.*166_*167del
ENST00000361915.7:c.*166_*167del ENSP00000355106.3:n.*166_*167del
ENST00000370161.6:c.4717_4718del ENSP00000359180.2:n.4717_4718del
ENST00000370163.7:c.*166_*167del ENSP00000359182.3:n.*166_*167del
ENST00000370165.7:c.*166_*167del ENSP00000359184.3:n.*166_*167del
NM_000028.2:c.*166_*167del NP_000019.2:n.*166_*167del
NM_000642.2:c.*166_*167del NP_000633.2:n.*166_*167del
NM_000643.2:c.*166_*167del NP_000634.2:n.*166_*167del
NM_000644.2:c.*166_*167del NP_000635.2:n.*166_*167del
NM_000645.2:c.*166_*167del NP_000636.2:n.*166_*167del
NM_000646.2:c.*166_*167del NP_000637.2:n.*166_*167del
XM_005270557.1:c.*166_*167del XP_005270614.1:n.*166_*167del
XR_947626.1:n.1317+2421_1317+2422del
XR_947627.1:n.1206+2421_1206+2422del
XR_947628.1:n.1311+2421_1311+2422del
XR_947630.1:n.1249+2421_1249+2422del
XR_947632.1:n.1135+2421_1135+2422del
XR_947633.1:n.1246+2421_1246+2422del
XR_947634.1:n.660+2421_660+2422del
XR_947635.1:n.728+2421_728+2422del
XM_005270557.2:c.*166_*167del XP_005270614.1:n.*166_*167del
XM_017000501.2:c.*166_*167del XP_016855990.1:n.*166_*167del
NM_000642.3:c.*166_*167del MANE Select NP_000633.2:n.*166_*167del