Canonical Allele Identifier: CA1183927304
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99876467T= , CM000663.2:g.99876467T= GRCh38
NC_000001.10:g.100342023T= , CM000663.1:g.100342023T= GRCh37
NC_000001.9:g.100114611T= NCBI36
NG_012865.1:g.31384T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.1293T= MANE Select ENSP00000355106.3:p.Thr431=
ENST00000637337.1:n.1504T=
ENST00000294724.8:c.1293T= ENSP00000294724.4:p.Thr431=
ENST00000361302.7:c.1245T= ENSP00000354971.3:p.Thr415=
ENST00000361522.4:c.1242T= ENSP00000354635.4:p.Thr414=
ENST00000361915.7:c.1293T= ENSP00000355106.3:p.Thr431=
ENST00000370161.6:c.1245T= ENSP00000359180.2:p.Thr415=
ENST00000370163.7:c.1293T= ENSP00000359182.3:p.Thr431=
ENST00000370165.7:c.1293T= ENSP00000359184.3:p.Thr431=
ENST00000477753.1:n.552T=
NM_000028.2:c.1293T= NP_000019.2:p.Thr431=
NM_000642.2:c.1293T= NP_000633.2:p.Thr431=
NM_000643.2:c.1293T= NP_000634.2:p.Thr431=
NM_000644.2:c.1293T= NP_000635.2:p.Thr431=
NM_000645.2:c.1242T= NP_000636.2:p.Thr414=
NM_000646.2:c.1245T= NP_000637.2:p.Thr415=
XM_005270557.1:c.1293T= XP_005270614.1:p.Thr431=
XM_005270557.2:c.1293T= XP_005270614.1:p.Thr431=
NM_000642.3:c.1293T= MANE Select NP_000633.2:p.Thr431=