Canonical Allele Identifier: CA1183945259
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99921987_99921992delinsTGAAAA , CM000663.2:g.99921987_99921992delinsTGAAAA GRCh38
NC_000001.10:g.100387543_100387548delinsTGAAAA , CM000663.1:g.100387543_100387548delinsTGAAAA GRCh37
NC_000001.9:g.100160131_100160136delinsTGAAAA NCBI36
NG_012865.1:g.76904_76909delinsTGAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.*336_*341delinsTGAAAA MANE Select ENSP00000355106.3:n.*336_*341delinsTGAAAA
ENST00000637337.1:n.5146_5151delinsTGAAAA
ENST00000294724.8:c.*336_*341delinsTGAAAA ENSP00000294724.4:n.*336_*341delinsTGAAAA
ENST00000361302.7:c.*336_*341delinsTGAAAA ENSP00000354971.3:n.*336_*341delinsTGAAAA
ENST00000361522.4:c.*336_*341delinsTGAAAA ENSP00000354635.4:n.*336_*341delinsTGAAAA
ENST00000361915.7:c.*336_*341delinsTGAAAA ENSP00000355106.3:n.*336_*341delinsTGAAAA
ENST00000370161.6:c.4887_4892delinsTGAAAA ENSP00000359180.2:n.4887_4892delinsTGAAAA
ENST00000370163.7:c.*336_*341delinsTGAAAA ENSP00000359182.3:n.*336_*341delinsTGAAAA
ENST00000370165.7:c.*336_*341delinsTGAAAA ENSP00000359184.3:n.*336_*341delinsTGAAAA
NM_000028.2:c.*336_*341delinsTGAAAA NP_000019.2:n.*336_*341delinsTGAAAA
NM_000642.2:c.*336_*341delinsTGAAAA NP_000633.2:n.*336_*341delinsTGAAAA
NM_000643.2:c.*336_*341delinsTGAAAA NP_000634.2:n.*336_*341delinsTGAAAA
NM_000644.2:c.*336_*341delinsTGAAAA NP_000635.2:n.*336_*341delinsTGAAAA
NM_000645.2:c.*336_*341delinsTGAAAA NP_000636.2:n.*336_*341delinsTGAAAA
NM_000646.2:c.*336_*341delinsTGAAAA NP_000637.2:n.*336_*341delinsTGAAAA
XM_005270557.1:c.*336_*341delinsTGAAAA XP_005270614.1:n.*336_*341delinsTGAAAA
XR_947626.1:n.1317+2246_1317+2251delinsTTTTCA
XR_947627.1:n.1206+2246_1206+2251delinsTTTTCA
XR_947628.1:n.1311+2246_1311+2251delinsTTTTCA
XR_947630.1:n.1249+2246_1249+2251delinsTTTTCA
XR_947632.1:n.1135+2246_1135+2251delinsTTTTCA
XR_947633.1:n.1246+2246_1246+2251delinsTTTTCA
XR_947634.1:n.660+2246_660+2251delinsTTTTCA
XR_947635.1:n.728+2246_728+2251delinsTTTTCA
XM_005270557.2:c.*336_*341delinsTGAAAA XP_005270614.1:n.*336_*341delinsTGAAAA
XM_017000501.2:c.*336_*341delinsTGAAAA XP_016855990.1:n.*336_*341delinsTGAAAA
NM_000642.3:c.*336_*341delinsTGAAAA MANE Select NP_000633.2:n.*336_*341delinsTGAAAA