Canonical Allele Identifier: CA1183917122
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99851110T= , CM000663.2:g.99851110T= GRCh38
NC_000001.10:g.100316666T= , CM000663.1:g.100316666T= GRCh37
NC_000001.9:g.100089254T= NCBI36
NG_012865.1:g.6027T=

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.68T= MANE Select ENSP00000355106.3:p.Phe23=
ENST00000294724.8:c.68T= ENSP00000294724.4:p.Phe23=
ENST00000361302.7:c.-124T= ENSP00000354971.3:n.-124T=
ENST00000361915.7:c.68T= ENSP00000355106.3:p.Phe23=
ENST00000370163.7:c.68T= ENSP00000359182.3:p.Phe23=
ENST00000370165.7:c.68T= ENSP00000359184.3:p.Phe23=
NM_000028.2:c.68T= NP_000019.2:p.Phe23=
NM_000642.2:c.68T= NP_000633.2:p.Phe23=
NM_000643.2:c.68T= NP_000634.2:p.Phe23=
NM_000644.2:c.68T= NP_000635.2:p.Phe23=
NM_000646.2:c.-124T= NP_000637.2:n.-124T=
XM_005270557.1:c.68T= XP_005270614.1:p.Phe23=
XM_005270557.2:c.68T= XP_005270614.1:p.Phe23=
NM_000642.3:c.68T= MANE Select NP_000633.2:p.Phe23=