Canonical Allele Identifier: CA2532930935
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99876664_99876688del , CM000663.2:g.99876664_99876688del GRCh38
NC_000001.10:g.100342220_100342244del , CM000663.1:g.100342220_100342244del GRCh37
NC_000001.9:g.100114808_100114832del NCBI36
NG_012865.1:g.31581_31605del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.1423+67_1423+91del MANE Select ENSP00000355106.3:n.1423+67_1423+91del
ENST00000637337.1:n.1634+67_1634+91del
ENST00000294724.8:c.1423+67_1423+91del ENSP00000294724.4:n.1423+67_1423+91del
ENST00000361302.7:c.1375+67_1375+91del ENSP00000354971.3:n.1375+67_1375+91del
ENST00000361522.4:c.1372+67_1372+91del ENSP00000354635.4:n.1372+67_1372+91del
ENST00000361915.7:c.1423+67_1423+91del ENSP00000355106.3:n.1423+67_1423+91del
ENST00000370161.6:c.1375+67_1375+91del ENSP00000359180.2:n.1375+67_1375+91del
ENST00000370163.7:c.1423+67_1423+91del ENSP00000359182.3:n.1423+67_1423+91del
ENST00000370165.7:c.1423+67_1423+91del ENSP00000359184.3:n.1423+67_1423+91del
NM_000028.2:c.1423+67_1423+91del NP_000019.2:n.1423+67_1423+91del
NM_000642.2:c.1423+67_1423+91del NP_000633.2:n.1423+67_1423+91del
NM_000643.2:c.1423+67_1423+91del NP_000634.2:n.1423+67_1423+91del
NM_000644.2:c.1423+67_1423+91del NP_000635.2:n.1423+67_1423+91del
NM_000645.2:c.1372+67_1372+91del NP_000636.2:n.1372+67_1372+91del
NM_000646.2:c.1375+67_1375+91del NP_000637.2:n.1375+67_1375+91del
XM_005270557.1:c.1423+67_1423+91del XP_005270614.1:n.1423+67_1423+91del
XM_005270557.2:c.1423+67_1423+91del XP_005270614.1:n.1423+67_1423+91del
NM_000642.3:c.1423+67_1423+91del MANE Select NP_000633.2:n.1423+67_1423+91del