Canonical Allele Identifier: CA1183926846
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99875396_99875400delinsACTGG , CM000663.2:g.99875396_99875400delinsACTGG GRCh38
NC_000001.10:g.100340952_100340956delinsACTGG , CM000663.1:g.100340952_100340956delinsACTGG GRCh37
NC_000001.9:g.100113540_100113544delinsACTGG NCBI36
NG_012865.1:g.30313_30317delinsACTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.1224_1228delinsACTGG MANE Select ENSP00000355106.3:p.Arg408=
ENST00000637337.1:n.1435_1439delinsACTGG
ENST00000294724.8:c.1224_1228delinsACTGG ENSP00000294724.4:p.Arg408=
ENST00000361302.7:c.1176_1180delinsACTGG ENSP00000354971.3:p.Arg392=
ENST00000361522.4:c.1173_1177delinsACTGG ENSP00000354635.4:p.Arg391=
ENST00000361915.7:c.1224_1228delinsACTGG ENSP00000355106.3:p.Arg408=
ENST00000370161.6:c.1176_1180delinsACTGG ENSP00000359180.2:p.Arg392=
ENST00000370163.7:c.1224_1228delinsACTGG ENSP00000359182.3:p.Arg408=
ENST00000370165.7:c.1224_1228delinsACTGG ENSP00000359184.3:p.Arg408=
ENST00000477753.1:n.483_487delinsACTGG
NM_000028.2:c.1224_1228delinsACTGG NP_000019.2:p.Arg408=
NM_000642.2:c.1224_1228delinsACTGG NP_000633.2:p.Arg408=
NM_000643.2:c.1224_1228delinsACTGG NP_000634.2:p.Arg408=
NM_000644.2:c.1224_1228delinsACTGG NP_000635.2:p.Arg408=
NM_000645.2:c.1173_1177delinsACTGG NP_000636.2:p.Arg391=
NM_000646.2:c.1176_1180delinsACTGG NP_000637.2:p.Arg392=
XM_005270557.1:c.1224_1228delinsACTGG XP_005270614.1:p.Arg408=
XM_005270557.2:c.1224_1228delinsACTGG XP_005270614.1:p.Arg408=
NM_000642.3:c.1224_1228delinsACTGG MANE Select NP_000633.2:p.Arg408=