Canonical Allele Identifier: CA2646737426
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99876666_99876667insAGAT , CM000663.2:g.99876666_99876667insAGAT GRCh38
NC_000001.10:g.100342222_100342223insAGAT , CM000663.1:g.100342222_100342223insAGAT GRCh37
NC_000001.9:g.100114810_100114811insAGAT NCBI36
NG_012865.1:g.31583_31584insAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.1423+69_1423+70insAGAT MANE Select ENSP00000355106.3:n.1423+69_1423+70insAGAT
ENST00000637337.1:n.1634+69_1634+70insAGAT
ENST00000294724.8:c.1423+69_1423+70insAGAT ENSP00000294724.4:n.1423+69_1423+70insAGAT
ENST00000361302.7:c.1375+69_1375+70insAGAT ENSP00000354971.3:n.1375+69_1375+70insAGAT
ENST00000361522.4:c.1372+69_1372+70insAGAT ENSP00000354635.4:n.1372+69_1372+70insAGAT
ENST00000361915.7:c.1423+69_1423+70insAGAT ENSP00000355106.3:n.1423+69_1423+70insAGAT
ENST00000370161.6:c.1375+69_1375+70insAGAT ENSP00000359180.2:n.1375+69_1375+70insAGAT
ENST00000370163.7:c.1423+69_1423+70insAGAT ENSP00000359182.3:n.1423+69_1423+70insAGAT
ENST00000370165.7:c.1423+69_1423+70insAGAT ENSP00000359184.3:n.1423+69_1423+70insAGAT
NM_000028.2:c.1423+69_1423+70insAGAT NP_000019.2:n.1423+69_1423+70insAGAT
NM_000642.2:c.1423+69_1423+70insAGAT NP_000633.2:n.1423+69_1423+70insAGAT
NM_000643.2:c.1423+69_1423+70insAGAT NP_000634.2:n.1423+69_1423+70insAGAT
NM_000644.2:c.1423+69_1423+70insAGAT NP_000635.2:n.1423+69_1423+70insAGAT
NM_000645.2:c.1372+69_1372+70insAGAT NP_000636.2:n.1372+69_1372+70insAGAT
NM_000646.2:c.1375+69_1375+70insAGAT NP_000637.2:n.1375+69_1375+70insAGAT
XM_005270557.1:c.1423+69_1423+70insAGAT XP_005270614.1:n.1423+69_1423+70insAGAT
XM_005270557.2:c.1423+69_1423+70insAGAT XP_005270614.1:n.1423+69_1423+70insAGAT
NM_000642.3:c.1423+69_1423+70insAGAT MANE Select NP_000633.2:n.1423+69_1423+70insAGAT