Canonical Allele Identifier: CA2646739657
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921856_99921932del , CM000663.2:g.99921856_99921932del GRCh38
NC_000001.10:g.100387412_100387488del , CM000663.1:g.100387412_100387488del GRCh37
NC_000001.9:g.100160000_100160076del NCBI36
NG_012865.1:g.76773_76849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*205_*281del MANE Select ENSP00000355106.3:n.*205_*281del
ENST00000637337.1:n.5015_5091del
ENST00000294724.8:c.*205_*281del ENSP00000294724.4:n.*205_*281del
ENST00000361302.7:c.*205_*281del ENSP00000354971.3:n.*205_*281del
ENST00000361522.4:c.*205_*281del ENSP00000354635.4:n.*205_*281del
ENST00000361915.7:c.*205_*281del ENSP00000355106.3:n.*205_*281del
ENST00000370161.6:c.4756_4832del ENSP00000359180.2:n.4756_4832del
ENST00000370163.7:c.*205_*281del ENSP00000359182.3:n.*205_*281del
ENST00000370165.7:c.*205_*281del ENSP00000359184.3:n.*205_*281del
NM_000028.2:c.*205_*281del NP_000019.2:n.*205_*281del
NM_000642.2:c.*205_*281del NP_000633.2:n.*205_*281del
NM_000643.2:c.*205_*281del NP_000634.2:n.*205_*281del
NM_000644.2:c.*205_*281del NP_000635.2:n.*205_*281del
NM_000645.2:c.*205_*281del NP_000636.2:n.*205_*281del
NM_000646.2:c.*205_*281del NP_000637.2:n.*205_*281del
XM_005270557.1:c.*205_*281del XP_005270614.1:n.*205_*281del
XR_947626.1:n.1317+2311_1317+2387del
XR_947627.1:n.1206+2311_1206+2387del
XR_947628.1:n.1311+2311_1311+2387del
XR_947630.1:n.1249+2311_1249+2387del
XR_947632.1:n.1135+2311_1135+2387del
XR_947633.1:n.1246+2311_1246+2387del
XR_947634.1:n.660+2311_660+2387del
XR_947635.1:n.728+2311_728+2387del
XM_005270557.2:c.*205_*281del XP_005270614.1:n.*205_*281del
XM_017000501.2:c.*205_*281del XP_016855990.1:n.*205_*281del
NM_000642.3:c.*205_*281del MANE Select NP_000633.2:n.*205_*281del