Canonical Allele Identifier: CA1183945242

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99921954_99921967delinsAATGAAAATAAAAT , CM000663.2:g.99921954_99921967delinsAATGAAAATAAAAT	GRCh38
NC_000001.10:g.100387510_100387523delinsAATGAAAATAAAAT , CM000663.1:g.100387510_100387523delinsAATGAAAATAAAAT	GRCh37
NC_000001.9:g.100160098_100160111delinsAATGAAAATAAAAT	NCBI36
NG_012865.1:g.76871_76884delinsAATGAAAATAAAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.*303_*316delinsAATGAAAATAAAAT MANE Select	ENSP00000355106.3:n.*303_*316delinsAATGAAAATAAAAT
ENST00000637337.1:n.5113_5126delinsAATGAAAATAAAAT
ENST00000294724.8:c.*303_*316delinsAATGAAAATAAAAT	ENSP00000294724.4:n.*303_*316delinsAATGAAAATAAAAT
ENST00000361302.7:c.*303_*316delinsAATGAAAATAAAAT	ENSP00000354971.3:n.*303_*316delinsAATGAAAATAAAAT
ENST00000361522.4:c.*303_*316delinsAATGAAAATAAAAT	ENSP00000354635.4:n.*303_*316delinsAATGAAAATAAAAT
ENST00000361915.7:c.*303_*316delinsAATGAAAATAAAAT	ENSP00000355106.3:n.*303_*316delinsAATGAAAATAAAAT
ENST00000370161.6:c.4854_4867delinsAATGAAAATAAAAT	ENSP00000359180.2:n.4854_4867delinsAATGAAAATAAAAT
ENST00000370163.7:c.*303_*316delinsAATGAAAATAAAAT	ENSP00000359182.3:n.*303_*316delinsAATGAAAATAAAAT
ENST00000370165.7:c.*303_*316delinsAATGAAAATAAAAT	ENSP00000359184.3:n.*303_*316delinsAATGAAAATAAAAT
NM_000028.2:c.*303_*316delinsAATGAAAATAAAAT	NP_000019.2:n.*303_*316delinsAATGAAAATAAAAT
NM_000642.2:c.*303_*316delinsAATGAAAATAAAAT	NP_000633.2:n.*303_*316delinsAATGAAAATAAAAT
NM_000643.2:c.*303_*316delinsAATGAAAATAAAAT	NP_000634.2:n.*303_*316delinsAATGAAAATAAAAT
NM_000644.2:c.*303_*316delinsAATGAAAATAAAAT	NP_000635.2:n.*303_*316delinsAATGAAAATAAAAT
NM_000645.2:c.*303_*316delinsAATGAAAATAAAAT	NP_000636.2:n.*303_*316delinsAATGAAAATAAAAT
NM_000646.2:c.*303_*316delinsAATGAAAATAAAAT	NP_000637.2:n.*303_*316delinsAATGAAAATAAAAT
XM_005270557.1:c.*303_*316delinsAATGAAAATAAAAT	XP_005270614.1:n.*303_*316delinsAATGAAAATAAAAT
XR_947626.1:n.1317+2271_1317+2284delinsATTTTATTTTCATT
XR_947627.1:n.1206+2271_1206+2284delinsATTTTATTTTCATT
XR_947628.1:n.1311+2271_1311+2284delinsATTTTATTTTCATT
XR_947630.1:n.1249+2271_1249+2284delinsATTTTATTTTCATT
XR_947632.1:n.1135+2271_1135+2284delinsATTTTATTTTCATT
XR_947633.1:n.1246+2271_1246+2284delinsATTTTATTTTCATT
XR_947634.1:n.660+2271_660+2284delinsATTTTATTTTCATT
XR_947635.1:n.728+2271_728+2284delinsATTTTATTTTCATT
XM_005270557.2:c.*303_*316delinsAATGAAAATAAAAT	XP_005270614.1:n.*303_*316delinsAATGAAAATAAAAT
XM_017000501.2:c.*303_*316delinsAATGAAAATAAAAT	XP_016855990.1:n.*303_*316delinsAATGAAAATAAAAT
NM_000642.3:c.*303_*316delinsAATGAAAATAAAAT MANE Select	NP_000633.2:n.*303_*316delinsAATGAAAATAAAAT