Canonical Allele Identifier: CA1183929259
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99881259G= , CM000663.2:g.99881259G= GRCh38
NC_000001.10:g.100346815G= , CM000663.1:g.100346815G= GRCh37
NC_000001.9:g.100119403G= NCBI36
NG_012865.1:g.36176G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.2002-33G= MANE Select ENSP00000355106.3:n.2002-33G=
ENST00000637337.1:n.2213-33G=
ENST00000294724.8:c.2002-33G= ENSP00000294724.4:n.2002-33G=
ENST00000361302.7:c.1954-33G= ENSP00000354971.3:n.1954-33G=
ENST00000361522.4:c.1951-33G= ENSP00000354635.4:n.1951-33G=
ENST00000361915.7:c.2002-33G= ENSP00000355106.3:n.2002-33G=
ENST00000370161.6:c.1954-33G= ENSP00000359180.2:n.1954-33G=
ENST00000370163.7:c.2002-33G= ENSP00000359182.3:n.2002-33G=
ENST00000370165.7:c.2002-33G= ENSP00000359184.3:n.2002-33G=
NM_000028.2:c.2002-33G= NP_000019.2:n.2002-33G=
NM_000642.2:c.2002-33G= NP_000633.2:n.2002-33G=
NM_000643.2:c.2002-33G= NP_000634.2:n.2002-33G=
NM_000644.2:c.2002-33G= NP_000635.2:n.2002-33G=
NM_000645.2:c.1951-33G= NP_000636.2:n.1951-33G=
NM_000646.2:c.1954-33G= NP_000637.2:n.1954-33G=
XM_005270557.1:c.2002-33G= XP_005270614.1:n.2002-33G=
XM_005270557.2:c.2002-33G= XP_005270614.1:n.2002-33G=
XM_017000501.2:c.262-33G= XP_016855990.1:n.262-33G=
NM_000642.3:c.2002-33G= MANE Select NP_000633.2:n.2002-33G=