Canonical Allele Identifier: CA2744753093
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99851006_99851012del , CM000663.2:g.99851006_99851012del GRCh38
NC_000001.10:g.100316562_100316568del , CM000663.1:g.100316562_100316568del GRCh37
NC_000001.9:g.100089150_100089156del NCBI36
NG_012865.1:g.5923_5929del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.-37_-31del MANE Select ENSP00000355106.3:n.-37_-31del
ENST00000294724.8:c.-37_-31del ENSP00000294724.4:n.-37_-31del
ENST00000361302.7:c.-228_-222del ENSP00000354971.3:n.-228_-222del
ENST00000361915.7:c.-37_-31del ENSP00000355106.3:n.-37_-31del
ENST00000370163.7:c.-37_-31del ENSP00000359182.3:n.-37_-31del
ENST00000370165.7:c.-8-29_-8-23del ENSP00000359184.3:n.-8-29_-8-23del
NM_000028.2:c.-37_-31del NP_000019.2:n.-37_-31del
NM_000642.2:c.-37_-31del NP_000633.2:n.-37_-31del
NM_000643.2:c.-37_-31del NP_000634.2:n.-37_-31del
NM_000644.2:c.-8-29_-8-23del NP_000635.2:n.-8-29_-8-23del
NM_000646.2:c.-228_-222del NP_000637.2:n.-228_-222del
XM_005270557.1:c.-37_-31del XP_005270614.1:n.-37_-31del
XM_005270557.2:c.-37_-31del XP_005270614.1:n.-37_-31del
NM_000642.3:c.-37_-31del MANE Select NP_000633.2:n.-37_-31del