Canonical Allele Identifier: CA1141373057
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99916704_99916706delinsTTT , CM000663.2:g.99916704_99916706delinsTTT GRCh38
NC_000001.10:g.100382260_100382262delinsTTT , CM000663.1:g.100382260_100382262delinsTTT GRCh37
NC_000001.9:g.100154848_100154850delinsTTT NCBI36
NG_012865.1:g.71621_71623delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.4454_4456delinsTTT MANE Select ENSP00000355106.3:p.Leu1485=
ENST00000637337.1:n.4665_4667delinsTTT
ENST00000294724.8:c.4454_4456delinsTTT ENSP00000294724.4:p.Leu1485=
ENST00000361302.7:c.4406_4408delinsTTT ENSP00000354971.3:p.Leu1469=
ENST00000361522.4:c.4403_4405delinsTTT ENSP00000354635.4:p.Leu1468=
ENST00000361915.7:c.4454_4456delinsTTT ENSP00000355106.3:p.Leu1485=
ENST00000370161.6:c.4406_4408delinsTTT ENSP00000359180.2:p.Leu1469=
ENST00000370163.7:c.4454_4456delinsTTT ENSP00000359182.3:p.Leu1485=
ENST00000370165.7:c.4454_4456delinsTTT ENSP00000359184.3:p.Leu1485=
NM_000028.2:c.4454_4456delinsTTT NP_000019.2:p.Leu1485=
NM_000642.2:c.4454_4456delinsTTT NP_000633.2:p.Leu1485=
NM_000643.2:c.4454_4456delinsTTT NP_000634.2:p.Leu1485=
NM_000644.2:c.4454_4456delinsTTT NP_000635.2:p.Leu1485=
NM_000645.2:c.4403_4405delinsTTT NP_000636.2:p.Leu1468=
NM_000646.2:c.4406_4408delinsTTT NP_000637.2:p.Leu1469=
XM_005270557.1:c.4454_4456delinsTTT XP_005270614.1:p.Leu1485=
XR_947626.1:n.1318-3489_1318-3487delinsAAA
XR_947627.1:n.1207-3489_1207-3487delinsAAA
XR_947628.1:n.1312-3489_1312-3487delinsAAA
XR_947630.1:n.1250-3489_1250-3487delinsAAA
XR_947632.1:n.1136-3489_1136-3487delinsAAA
XR_947633.1:n.1247-3489_1247-3487delinsAAA
XR_947634.1:n.661-3489_661-3487delinsAAA
XR_947635.1:n.729-3489_729-3487delinsAAA
XM_005270557.2:c.4454_4456delinsTTT XP_005270614.1:p.Leu1485=
XM_017000501.2:c.2714_2716delinsTTT XP_016855990.1:p.Leu905=
NM_000642.3:c.4454_4456delinsTTT MANE Select NP_000633.2:p.Leu1485=