Canonical Allele Identifier: CA2646734405
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99861496dup , CM000663.2:g.99861496dup GRCh38
NC_000001.10:g.100327052dup , CM000663.1:g.100327052dup GRCh37
NC_000001.9:g.100099640dup NCBI36
NG_012865.1:g.16413dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.83-7dup MANE Select ENSP00000355106.3:n.83-7dup
ENST00000637337.1:n.287dup
ENST00000294724.8:c.83-7dup ENSP00000294724.4:n.83-7dup
ENST00000361302.7:c.35-7dup ENSP00000354971.3:n.35-7dup
ENST00000361522.4:c.25dup ENSP00000354635.4:p.Tyr9LeufsTer5
ENST00000361915.7:c.83-7dup ENSP00000355106.3:n.83-7dup
ENST00000370161.6:c.35-7dup ENSP00000359180.2:n.35-7dup
ENST00000370163.7:c.83-7dup ENSP00000359182.3:n.83-7dup
ENST00000370165.7:c.83-7dup ENSP00000359184.3:n.83-7dup
NM_000028.2:c.83-7dup NP_000019.2:n.83-7dup
NM_000642.2:c.83-7dup NP_000633.2:n.83-7dup
NM_000643.2:c.83-7dup NP_000634.2:n.83-7dup
NM_000644.2:c.83-7dup NP_000635.2:n.83-7dup
NM_000645.2:c.25dup NP_000636.2:p.Tyr9LeufsTer5
NM_000646.2:c.35-7dup NP_000637.2:n.35-7dup
XM_005270557.1:c.83-7dup XP_005270614.1:n.83-7dup
XM_005270557.2:c.83-7dup XP_005270614.1:n.83-7dup
NM_000642.3:c.83-7dup MANE Select NP_000633.2:n.83-7dup