Canonical Allele Identifier: CA1183941766
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99910897_99910901delinsCACTT , CM000663.2:g.99910897_99910901delinsCACTT GRCh38
NC_000001.10:g.100376453_100376457delinsCACTT , CM000663.1:g.100376453_100376457delinsCACTT GRCh37
NC_000001.9:g.100149041_100149045delinsCACTT NCBI36
NG_012865.1:g.65814_65818delinsCACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.3836+50_3836+54delinsCACTT MANE Select ENSP00000355106.3:n.3836+50_3836+54delinsCACTT
ENST00000637337.1:n.4047+50_4047+54delinsCACTT
ENST00000294724.8:c.3836+50_3836+54delinsCACTT ENSP00000294724.4:n.3836+50_3836+54delinsCACTT
ENST00000361302.7:c.3788+50_3788+54delinsCACTT ENSP00000354971.3:n.3788+50_3788+54delinsCACTT
ENST00000361522.4:c.3785+50_3785+54delinsCACTT ENSP00000354635.4:n.3785+50_3785+54delinsCACTT
ENST00000361915.7:c.3836+50_3836+54delinsCACTT ENSP00000355106.3:n.3836+50_3836+54delinsCACTT
ENST00000370161.6:c.3788+50_3788+54delinsCACTT ENSP00000359180.2:n.3788+50_3788+54delinsCACTT
ENST00000370163.7:c.3836+50_3836+54delinsCACTT ENSP00000359182.3:n.3836+50_3836+54delinsCACTT
ENST00000370165.7:c.3836+50_3836+54delinsCACTT ENSP00000359184.3:n.3836+50_3836+54delinsCACTT
NM_000028.2:c.3836+50_3836+54delinsCACTT NP_000019.2:n.3836+50_3836+54delinsCACTT
NM_000642.2:c.3836+50_3836+54delinsCACTT NP_000633.2:n.3836+50_3836+54delinsCACTT
NM_000643.2:c.3836+50_3836+54delinsCACTT NP_000634.2:n.3836+50_3836+54delinsCACTT
NM_000644.2:c.3836+50_3836+54delinsCACTT NP_000635.2:n.3836+50_3836+54delinsCACTT
NM_000645.2:c.3785+50_3785+54delinsCACTT NP_000636.2:n.3785+50_3785+54delinsCACTT
NM_000646.2:c.3788+50_3788+54delinsCACTT NP_000637.2:n.3788+50_3788+54delinsCACTT
XM_005270557.1:c.3836+50_3836+54delinsCACTT XP_005270614.1:n.3836+50_3836+54delinsCACTT
XM_005270557.2:c.3836+50_3836+54delinsCACTT XP_005270614.1:n.3836+50_3836+54delinsCACTT
XM_017000501.2:c.2096+50_2096+54delinsCACTT XP_016855990.1:n.2096+50_2096+54delinsCACTT
NM_000642.3:c.3836+50_3836+54delinsCACTT MANE Select NP_000633.2:n.3836+50_3836+54delinsCACTT