Canonical Allele Identifier: CA1183927433
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99876771_99876774delinsAAAG , CM000663.2:g.99876771_99876774delinsAAAG GRCh38
NC_000001.10:g.100342327_100342330delinsAAAG , CM000663.1:g.100342327_100342330delinsAAAG GRCh37
NC_000001.9:g.100114915_100114918delinsAAAG NCBI36
NG_012865.1:g.31688_31691delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.1423+174_1423+177delinsAAAG MANE Select ENSP00000355106.3:n.1423+174_1423+177delinsAAAG
ENST00000637337.1:n.1634+174_1634+177delinsAAAG
ENST00000294724.8:c.1423+174_1423+177delinsAAAG ENSP00000294724.4:n.1423+174_1423+177delinsAAAG
ENST00000361302.7:c.1375+174_1375+177delinsAAAG ENSP00000354971.3:n.1375+174_1375+177delinsAAAG
ENST00000361522.4:c.1372+174_1372+177delinsAAAG ENSP00000354635.4:n.1372+174_1372+177delinsAAAG
ENST00000361915.7:c.1423+174_1423+177delinsAAAG ENSP00000355106.3:n.1423+174_1423+177delinsAAAG
ENST00000370161.6:c.1375+174_1375+177delinsAAAG ENSP00000359180.2:n.1375+174_1375+177delinsAAAG
ENST00000370163.7:c.1423+174_1423+177delinsAAAG ENSP00000359182.3:n.1423+174_1423+177delinsAAAG
ENST00000370165.7:c.1423+174_1423+177delinsAAAG ENSP00000359184.3:n.1423+174_1423+177delinsAAAG
NM_000028.2:c.1423+174_1423+177delinsAAAG NP_000019.2:n.1423+174_1423+177delinsAAAG
NM_000642.2:c.1423+174_1423+177delinsAAAG NP_000633.2:n.1423+174_1423+177delinsAAAG
NM_000643.2:c.1423+174_1423+177delinsAAAG NP_000634.2:n.1423+174_1423+177delinsAAAG
NM_000644.2:c.1423+174_1423+177delinsAAAG NP_000635.2:n.1423+174_1423+177delinsAAAG
NM_000645.2:c.1372+174_1372+177delinsAAAG NP_000636.2:n.1372+174_1372+177delinsAAAG
NM_000646.2:c.1375+174_1375+177delinsAAAG NP_000637.2:n.1375+174_1375+177delinsAAAG
XM_005270557.1:c.1423+174_1423+177delinsAAAG XP_005270614.1:n.1423+174_1423+177delinsAAAG
XM_005270557.2:c.1423+174_1423+177delinsAAAG XP_005270614.1:n.1423+174_1423+177delinsAAAG
NM_000642.3:c.1423+174_1423+177delinsAAAG MANE Select NP_000633.2:n.1423+174_1423+177delinsAAAG