Canonical Allele Identifier: CA1183945028
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921676_99921680delinsATTAC , CM000663.2:g.99921676_99921680delinsATTAC GRCh38
NC_000001.10:g.100387232_100387236delinsATTAC , CM000663.1:g.100387232_100387236delinsATTAC GRCh37
NC_000001.9:g.100159820_100159824delinsATTAC NCBI36
NG_012865.1:g.76593_76597delinsATTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*25_*29delinsATTAC MANE Select ENSP00000355106.3:n.*25_*29delinsATTAC
ENST00000637337.1:n.4835_4839delinsATTAC
ENST00000294724.8:c.*25_*29delinsATTAC ENSP00000294724.4:n.*25_*29delinsATTAC
ENST00000361302.7:c.*25_*29delinsATTAC ENSP00000354971.3:n.*25_*29delinsATTAC
ENST00000361522.4:c.*25_*29delinsATTAC ENSP00000354635.4:n.*25_*29delinsATTAC
ENST00000361915.7:c.*25_*29delinsATTAC ENSP00000355106.3:n.*25_*29delinsATTAC
ENST00000370161.6:c.4576_4580delinsATTAC ENSP00000359180.2:n.4576_4580delinsATTAC
ENST00000370163.7:c.*25_*29delinsATTAC ENSP00000359182.3:n.*25_*29delinsATTAC
ENST00000370165.7:c.*25_*29delinsATTAC ENSP00000359184.3:n.*25_*29delinsATTAC
NM_000028.2:c.*25_*29delinsATTAC NP_000019.2:n.*25_*29delinsATTAC
NM_000642.2:c.*25_*29delinsATTAC NP_000633.2:n.*25_*29delinsATTAC
NM_000643.2:c.*25_*29delinsATTAC NP_000634.2:n.*25_*29delinsATTAC
NM_000644.2:c.*25_*29delinsATTAC NP_000635.2:n.*25_*29delinsATTAC
NM_000645.2:c.*25_*29delinsATTAC NP_000636.2:n.*25_*29delinsATTAC
NM_000646.2:c.*25_*29delinsATTAC NP_000637.2:n.*25_*29delinsATTAC
XM_005270557.1:c.*25_*29delinsATTAC XP_005270614.1:n.*25_*29delinsATTAC
XR_947626.1:n.1317+2558_1317+2562delinsGTAAT
XR_947627.1:n.1206+2558_1206+2562delinsGTAAT
XR_947628.1:n.1311+2558_1311+2562delinsGTAAT
XR_947630.1:n.1249+2558_1249+2562delinsGTAAT
XR_947632.1:n.1135+2558_1135+2562delinsGTAAT
XR_947633.1:n.1246+2558_1246+2562delinsGTAAT
XR_947634.1:n.660+2558_660+2562delinsGTAAT
XR_947635.1:n.728+2558_728+2562delinsGTAAT
XM_005270557.2:c.*25_*29delinsATTAC XP_005270614.1:n.*25_*29delinsATTAC
XM_017000501.2:c.*25_*29delinsATTAC XP_016855990.1:n.*25_*29delinsATTAC
NM_000642.3:c.*25_*29delinsATTAC MANE Select NP_000633.2:n.*25_*29delinsATTAC