Canonical Allele Identifier: CA2574444945
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99916388_99916389del , CM000663.2:g.99916388_99916389del GRCh38
NC_000001.10:g.100381944_100381945del , CM000663.1:g.100381944_100381945del GRCh37
NC_000001.9:g.100154532_100154533del NCBI36
NG_012865.1:g.71305_71306del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.4260-22_4260-21del MANE Select ENSP00000355106.3:n.4260-22_4260-21del
ENST00000637337.1:n.4471-22_4471-21del
ENST00000294724.8:c.4260-22_4260-21del ENSP00000294724.4:n.4260-22_4260-21del
ENST00000361302.7:c.4212-22_4212-21del ENSP00000354971.3:n.4212-22_4212-21del
ENST00000361522.4:c.4209-22_4209-21del ENSP00000354635.4:n.4209-22_4209-21del
ENST00000361915.7:c.4260-22_4260-21del ENSP00000355106.3:n.4260-22_4260-21del
ENST00000370161.6:c.4212-22_4212-21del ENSP00000359180.2:n.4212-22_4212-21del
ENST00000370163.7:c.4260-22_4260-21del ENSP00000359182.3:n.4260-22_4260-21del
ENST00000370165.7:c.4260-22_4260-21del ENSP00000359184.3:n.4260-22_4260-21del
NM_000028.2:c.4260-22_4260-21del NP_000019.2:n.4260-22_4260-21del
NM_000642.2:c.4260-22_4260-21del NP_000633.2:n.4260-22_4260-21del
NM_000643.2:c.4260-22_4260-21del NP_000634.2:n.4260-22_4260-21del
NM_000644.2:c.4260-22_4260-21del NP_000635.2:n.4260-22_4260-21del
NM_000645.2:c.4209-22_4209-21del NP_000636.2:n.4209-22_4209-21del
NM_000646.2:c.4212-22_4212-21del NP_000637.2:n.4212-22_4212-21del
XM_005270557.1:c.4260-22_4260-21del XP_005270614.1:n.4260-22_4260-21del
XR_947626.1:n.1318-3172_1318-3171del
XR_947627.1:n.1207-3172_1207-3171del
XR_947628.1:n.1312-3172_1312-3171del
XR_947630.1:n.1250-3172_1250-3171del
XR_947632.1:n.1136-3172_1136-3171del
XR_947633.1:n.1247-3172_1247-3171del
XR_947634.1:n.661-3172_661-3171del
XR_947635.1:n.729-3172_729-3171del
XM_005270557.2:c.4260-22_4260-21del XP_005270614.1:n.4260-22_4260-21del
XM_017000501.2:c.2520-22_2520-21del XP_016855990.1:n.2520-22_2520-21del
NM_000642.3:c.4260-22_4260-21del MANE Select NP_000633.2:n.4260-22_4260-21del