Canonical Allele Identifier: CA2646739722
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921922_99921923insAAAAA , CM000663.2:g.99921922_99921923insAAAAA GRCh38
NC_000001.10:g.100387478_100387479insAAAAA , CM000663.1:g.100387478_100387479insAAAAA GRCh37
NC_000001.9:g.100160066_100160067insAAAAA NCBI36
NG_012865.1:g.76839_76840insAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*271_*272insAAAAA MANE Select ENSP00000355106.3:n.*271_*272insAAAAA
ENST00000637337.1:n.5081_5082insAAAAA
ENST00000294724.8:c.*271_*272insAAAAA ENSP00000294724.4:n.*271_*272insAAAAA
ENST00000361302.7:c.*271_*272insAAAAA ENSP00000354971.3:n.*271_*272insAAAAA
ENST00000361522.4:c.*271_*272insAAAAA ENSP00000354635.4:n.*271_*272insAAAAA
ENST00000361915.7:c.*271_*272insAAAAA ENSP00000355106.3:n.*271_*272insAAAAA
ENST00000370161.6:c.4822_4823insAAAAA ENSP00000359180.2:n.4822_4823insAAAAA
ENST00000370163.7:c.*271_*272insAAAAA ENSP00000359182.3:n.*271_*272insAAAAA
ENST00000370165.7:c.*271_*272insAAAAA ENSP00000359184.3:n.*271_*272insAAAAA
NM_000028.2:c.*271_*272insAAAAA NP_000019.2:n.*271_*272insAAAAA
NM_000642.2:c.*271_*272insAAAAA NP_000633.2:n.*271_*272insAAAAA
NM_000643.2:c.*271_*272insAAAAA NP_000634.2:n.*271_*272insAAAAA
NM_000644.2:c.*271_*272insAAAAA NP_000635.2:n.*271_*272insAAAAA
NM_000645.2:c.*271_*272insAAAAA NP_000636.2:n.*271_*272insAAAAA
NM_000646.2:c.*271_*272insAAAAA NP_000637.2:n.*271_*272insAAAAA
XM_005270557.1:c.*271_*272insAAAAA XP_005270614.1:n.*271_*272insAAAAA
XR_947626.1:n.1317+2319_1317+2320insTTTTT
XR_947627.1:n.1206+2319_1206+2320insTTTTT
XR_947628.1:n.1311+2319_1311+2320insTTTTT
XR_947630.1:n.1249+2319_1249+2320insTTTTT
XR_947632.1:n.1135+2319_1135+2320insTTTTT
XR_947633.1:n.1246+2319_1246+2320insTTTTT
XR_947634.1:n.660+2319_660+2320insTTTTT
XR_947635.1:n.728+2319_728+2320insTTTTT
XM_005270557.2:c.*271_*272insAAAAA XP_005270614.1:n.*271_*272insAAAAA
XM_017000501.2:c.*271_*272insAAAAA XP_016855990.1:n.*271_*272insAAAAA
NM_000642.3:c.*271_*272insAAAAA MANE Select NP_000633.2:n.*271_*272insAAAAA