Canonical Allele Identifier: CA1004961885
Gene: AGL HGNC NCBI

Linked Data

dbSNP Id: rs1655527251

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921753_99921754del , CM000663.2:g.99921753_99921754del GRCh38
NC_000001.10:g.100387309_100387310del , CM000663.1:g.100387309_100387310del GRCh37
NC_000001.9:g.100159897_100159898del NCBI36
NG_012865.1:g.76670_76671del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*102_*103del MANE Select ENSP00000355106.3:n.*102_*103del
ENST00000637337.1:n.4912_4913del
ENST00000294724.8:c.*102_*103del ENSP00000294724.4:n.*102_*103del
ENST00000361302.7:c.*102_*103del ENSP00000354971.3:n.*102_*103del
ENST00000361522.4:c.*102_*103del ENSP00000354635.4:n.*102_*103del
ENST00000361915.7:c.*102_*103del ENSP00000355106.3:n.*102_*103del
ENST00000370161.6:c.4653_4654del ENSP00000359180.2:n.4653_4654del
ENST00000370163.7:c.*102_*103del ENSP00000359182.3:n.*102_*103del
ENST00000370165.7:c.*102_*103del ENSP00000359184.3:n.*102_*103del
NM_000028.2:c.*102_*103del NP_000019.2:n.*102_*103del
NM_000642.2:c.*102_*103del NP_000633.2:n.*102_*103del
NM_000643.2:c.*102_*103del NP_000634.2:n.*102_*103del
NM_000644.2:c.*102_*103del NP_000635.2:n.*102_*103del
NM_000645.2:c.*102_*103del NP_000636.2:n.*102_*103del
NM_000646.2:c.*102_*103del NP_000637.2:n.*102_*103del
XM_005270557.1:c.*102_*103del XP_005270614.1:n.*102_*103del
XR_947626.1:n.1317+2484_1317+2485del
XR_947627.1:n.1206+2484_1206+2485del
XR_947628.1:n.1311+2484_1311+2485del
XR_947630.1:n.1249+2484_1249+2485del
XR_947632.1:n.1135+2484_1135+2485del
XR_947633.1:n.1246+2484_1246+2485del
XR_947634.1:n.660+2484_660+2485del
XR_947635.1:n.728+2484_728+2485del
XM_005270557.2:c.*102_*103del XP_005270614.1:n.*102_*103del
XM_017000501.2:c.*102_*103del XP_016855990.1:n.*102_*103del
NM_000642.3:c.*102_*103del MANE Select NP_000633.2:n.*102_*103del