Canonical Allele Identifier: CA1144191163
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99880593A= , CM000663.2:g.99880593A= GRCh38
NC_000001.10:g.100346149A= , CM000663.1:g.100346149A= GRCh37
NC_000001.9:g.100118737A= NCBI36
NG_012865.1:g.35510A=

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.1736-39A= MANE Select ENSP00000355106.3:n.1736-39A=
ENST00000637337.1:n.1947-39A=
ENST00000294724.8:c.1736-39A= ENSP00000294724.4:n.1736-39A=
ENST00000361302.7:c.1688-39A= ENSP00000354971.3:n.1688-39A=
ENST00000361522.4:c.1685-39A= ENSP00000354635.4:n.1685-39A=
ENST00000361915.7:c.1736-39A= ENSP00000355106.3:n.1736-39A=
ENST00000370161.6:c.1688-39A= ENSP00000359180.2:n.1688-39A=
ENST00000370163.7:c.1736-39A= ENSP00000359182.3:n.1736-39A=
ENST00000370165.7:c.1736-39A= ENSP00000359184.3:n.1736-39A=
NM_000028.2:c.1736-39A= NP_000019.2:n.1736-39A=
NM_000642.2:c.1736-39A= NP_000633.2:n.1736-39A=
NM_000643.2:c.1736-39A= NP_000634.2:n.1736-39A=
NM_000644.2:c.1736-39A= NP_000635.2:n.1736-39A=
NM_000645.2:c.1685-39A= NP_000636.2:n.1685-39A=
NM_000646.2:c.1688-39A= NP_000637.2:n.1688-39A=
XM_005270557.1:c.1736-39A= XP_005270614.1:n.1736-39A=
XM_005270557.2:c.1736-39A= XP_005270614.1:n.1736-39A=
XM_017000501.2:c.-5-39A= XP_016855990.1:n.-5-39A=
NM_000642.3:c.1736-39A= MANE Select NP_000633.2:n.1736-39A=