Canonical Allele Identifier: CA2646739556
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921695_99921696insA , CM000663.2:g.99921695_99921696insA GRCh38
NC_000001.10:g.100387251_100387252insA , CM000663.1:g.100387251_100387252insA GRCh37
NC_000001.9:g.100159839_100159840insA NCBI36
NG_012865.1:g.76612_76613insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*44_*45insA MANE Select ENSP00000355106.3:n.*44_*45insA
ENST00000637337.1:n.4854_4855insA
ENST00000294724.8:c.*44_*45insA ENSP00000294724.4:n.*44_*45insA
ENST00000361302.7:c.*44_*45insA ENSP00000354971.3:n.*44_*45insA
ENST00000361522.4:c.*44_*45insA ENSP00000354635.4:n.*44_*45insA
ENST00000361915.7:c.*44_*45insA ENSP00000355106.3:n.*44_*45insA
ENST00000370161.6:c.4595_4596insA ENSP00000359180.2:n.4595_4596insA
ENST00000370163.7:c.*44_*45insA ENSP00000359182.3:n.*44_*45insA
ENST00000370165.7:c.*44_*45insA ENSP00000359184.3:n.*44_*45insA
NM_000028.2:c.*44_*45insA NP_000019.2:n.*44_*45insA
NM_000642.2:c.*44_*45insA NP_000633.2:n.*44_*45insA
NM_000643.2:c.*44_*45insA NP_000634.2:n.*44_*45insA
NM_000644.2:c.*44_*45insA NP_000635.2:n.*44_*45insA
NM_000645.2:c.*44_*45insA NP_000636.2:n.*44_*45insA
NM_000646.2:c.*44_*45insA NP_000637.2:n.*44_*45insA
XM_005270557.1:c.*44_*45insA XP_005270614.1:n.*44_*45insA
XR_947626.1:n.1317+2542_1317+2543insT
XR_947627.1:n.1206+2542_1206+2543insT
XR_947628.1:n.1311+2542_1311+2543insT
XR_947630.1:n.1249+2542_1249+2543insT
XR_947632.1:n.1135+2542_1135+2543insT
XR_947633.1:n.1246+2542_1246+2543insT
XR_947634.1:n.660+2542_660+2543insT
XR_947635.1:n.728+2542_728+2543insT
XM_005270557.2:c.*44_*45insA XP_005270614.1:n.*44_*45insA
XM_017000501.2:c.*44_*45insA XP_016855990.1:n.*44_*45insA
NM_000642.3:c.*44_*45insA MANE Select NP_000633.2:n.*44_*45insA