Canonical Allele Identifier: CA1183938123
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99902641T= , CM000663.2:g.99902641T= GRCh38
NC_000001.10:g.100368197T= , CM000663.1:g.100368197T= GRCh37
NC_000001.9:g.100140785T= NCBI36
NG_012865.1:g.57558T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.3589-42T= MANE Select ENSP00000355106.3:n.3589-42T=
ENST00000637337.1:n.3800-42T=
ENST00000294724.8:c.3589-42T= ENSP00000294724.4:n.3589-42T=
ENST00000361302.7:c.3541-42T= ENSP00000354971.3:n.3541-42T=
ENST00000361522.4:c.3538-42T= ENSP00000354635.4:n.3538-42T=
ENST00000361915.7:c.3589-42T= ENSP00000355106.3:n.3589-42T=
ENST00000370161.6:c.3541-42T= ENSP00000359180.2:n.3541-42T=
ENST00000370163.7:c.3589-42T= ENSP00000359182.3:n.3589-42T=
ENST00000370165.7:c.3589-42T= ENSP00000359184.3:n.3589-42T=
NM_000028.2:c.3589-42T= NP_000019.2:n.3589-42T=
NM_000642.2:c.3589-42T= NP_000633.2:n.3589-42T=
NM_000643.2:c.3589-42T= NP_000634.2:n.3589-42T=
NM_000644.2:c.3589-42T= NP_000635.2:n.3589-42T=
NM_000645.2:c.3538-42T= NP_000636.2:n.3538-42T=
NM_000646.2:c.3541-42T= NP_000637.2:n.3541-42T=
XM_005270557.1:c.3589-42T= XP_005270614.1:n.3589-42T=
XM_005270557.2:c.3589-42T= XP_005270614.1:n.3589-42T=
XM_017000501.2:c.1849-42T= XP_016855990.1:n.1849-42T=
NM_000642.3:c.3589-42T= MANE Select NP_000633.2:n.3589-42T=