Canonical Allele Identifier: CA1183917080
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99851014G= , CM000663.2:g.99851014G= GRCh38
NC_000001.10:g.100316570G= , CM000663.1:g.100316570G= GRCh37
NC_000001.9:g.100089158G= NCBI36
NG_012865.1:g.5931G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.-29G= MANE Select ENSP00000355106.3:n.-29G=
ENST00000294724.8:c.-29G= ENSP00000294724.4:n.-29G=
ENST00000361302.7:c.-220G= ENSP00000354971.3:n.-220G=
ENST00000361915.7:c.-29G= ENSP00000355106.3:n.-29G=
ENST00000370163.7:c.-29G= ENSP00000359182.3:n.-29G=
ENST00000370165.7:c.-8-21G= ENSP00000359184.3:n.-8-21G=
NM_000028.2:c.-29G= NP_000019.2:n.-29G=
NM_000642.2:c.-29G= NP_000633.2:n.-29G=
NM_000643.2:c.-29G= NP_000634.2:n.-29G=
NM_000644.2:c.-8-21G= NP_000635.2:n.-8-21G=
NM_000646.2:c.-220G= NP_000637.2:n.-220G=
XM_005270557.1:c.-29G= XP_005270614.1:n.-29G=
XM_005270557.2:c.-29G= XP_005270614.1:n.-29G=
NM_000642.3:c.-29G= MANE Select NP_000633.2:n.-29G=