Canonical Allele Identifier: CA501114
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99914624_99916529del , CM000663.2:g.99914624_99916529del GRCh38
NC_000001.10:g.100380180_100382085del , CM000663.1:g.100380180_100382085del GRCh37
NC_000001.9:g.100152768_100154673del NCBI36
NG_012865.1:g.69541_71446del

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.4162-765_4347+32del
ENST00000637337.1:n.4373-765_4558+32del
ENST00000294724.8:c.4162-765_4347+32del
ENST00000361302.7:c.4114-765_4299+32del
ENST00000361522.4:c.4111-765_4296+32del
ENST00000361915.7:c.4162-765_4347+32del
ENST00000370161.6:c.4114-765_4299+32del
ENST00000370163.7:c.4162-765_4347+32del
ENST00000370165.7:c.4162-765_4347+32del
NM_000028.2:c.4162-765_4347+32del
NM_000642.2:c.4162-765_4347+32del
NM_000643.2:c.4162-765_4347+32del
NM_000644.2:c.4162-765_4347+32del
NM_000645.2:c.4111-765_4296+32del
NM_000646.2:c.4114-765_4299+32del
XM_005270557.1:c.4162-765_4347+32del
XR_947626.1:n.1318-3312_1318-1407del
XR_947627.1:n.1207-3312_1207-1407del
XR_947628.1:n.1312-3312_1312-1407del
XR_947630.1:n.1250-3312_1250-1407del
XR_947632.1:n.1136-3312_1136-1407del
XR_947633.1:n.1247-3312_1247-1407del
XR_947634.1:n.661-3312_661-1407del
XR_947635.1:n.729-3312_729-1407del
XM_005270557.2:c.4162-765_4347+32del
XM_017000501.2:c.2422-765_2607+32del
NM_000642.3:c.4162-765_4347+32del