Canonical Allele Identifier: CA2602458155
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921631_99921636del , CM000663.2:g.99921631_99921636del GRCh38
NC_000001.10:g.100387187_100387192del , CM000663.1:g.100387187_100387192del GRCh37
NC_000001.9:g.100159775_100159780del NCBI36
NG_012865.1:g.76548_76553del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.4579_4584del MANE Select ENSP00000355106.3:p.Glu1527_Thr1528del
ENST00000637337.1:n.4790_4795del
ENST00000294724.8:c.4579_4584del ENSP00000294724.4:p.Glu1527_Thr1528del
ENST00000361302.7:c.4531_4536del ENSP00000354971.3:p.Glu1511_Thr1512del
ENST00000361522.4:c.4528_4533del ENSP00000354635.4:p.Glu1510_Thr1511del
ENST00000361915.7:c.4579_4584del ENSP00000355106.3:p.Glu1527_Thr1528del
ENST00000370161.6:c.4531_4536del ENSP00000359180.2:p.Glu1511_Thr1512del
ENST00000370163.7:c.4579_4584del ENSP00000359182.3:p.Glu1527_Thr1528del
ENST00000370165.7:c.4579_4584del ENSP00000359184.3:p.Glu1527_Thr1528del
NM_000028.2:c.4579_4584del NP_000019.2:p.Glu1527_Thr1528del
NM_000642.2:c.4579_4584del NP_000633.2:p.Glu1527_Thr1528del
NM_000643.2:c.4579_4584del NP_000634.2:p.Glu1527_Thr1528del
NM_000644.2:c.4579_4584del NP_000635.2:p.Glu1527_Thr1528del
NM_000645.2:c.4528_4533del NP_000636.2:p.Glu1510_Thr1511del
NM_000646.2:c.4531_4536del NP_000637.2:p.Glu1511_Thr1512del
XM_005270557.1:c.4579_4584del XP_005270614.1:p.Glu1527_Thr1528del
XR_947626.1:n.1317+2602_1317+2607del
XR_947627.1:n.1206+2602_1206+2607del
XR_947628.1:n.1311+2602_1311+2607del
XR_947630.1:n.1249+2602_1249+2607del
XR_947632.1:n.1135+2602_1135+2607del
XR_947633.1:n.1246+2602_1246+2607del
XR_947634.1:n.660+2602_660+2607del
XR_947635.1:n.728+2602_728+2607del
XM_005270557.2:c.4579_4584del XP_005270614.1:p.Glu1527_Thr1528del
XM_017000501.2:c.2839_2844del XP_016855990.1:p.Glu947_Thr948del
NM_000642.3:c.4579_4584del MANE Select NP_000633.2:p.Glu1527_Thr1528del