Canonical Allele Identifier: CA2744755502
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99870453_99870465del , CM000663.2:g.99870453_99870465del GRCh38
NC_000001.10:g.100336009_100336021del , CM000663.1:g.100336009_100336021del GRCh37
NC_000001.9:g.100108597_100108609del NCBI36
NG_012865.1:g.25370_25382del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.718_730del MANE Select ENSP00000355106.3:p.Asn240Ter
ENST00000637337.1:n.929_941del
ENST00000294724.8:c.718_730del ENSP00000294724.4:p.Asn240Ter
ENST00000361302.7:c.670_682del ENSP00000354971.3:p.Asn224Ter
ENST00000361522.4:c.667_679del ENSP00000354635.4:p.Asn223Ter
ENST00000361915.7:c.718_730del ENSP00000355106.3:p.Asn240Ter
ENST00000370161.6:c.670_682del ENSP00000359180.2:p.Asn224Ter
ENST00000370163.7:c.718_730del ENSP00000359182.3:p.Asn240Ter
ENST00000370165.7:c.718_730del ENSP00000359184.3:p.Asn240Ter
NM_000028.2:c.718_730del NP_000019.2:p.Asn240Ter
NM_000642.2:c.718_730del NP_000633.2:p.Asn240Ter
NM_000643.2:c.718_730del NP_000634.2:p.Asn240Ter
NM_000644.2:c.718_730del NP_000635.2:p.Asn240Ter
NM_000645.2:c.667_679del NP_000636.2:p.Asn223Ter
NM_000646.2:c.670_682del NP_000637.2:p.Asn224Ter
XM_005270557.1:c.718_730del XP_005270614.1:p.Asn240Ter
XM_005270557.2:c.718_730del XP_005270614.1:p.Asn240Ter
NM_000642.3:c.718_730del MANE Select NP_000633.2:p.Asn240Ter