Canonical Allele Identifier: CA341323854
Gene: AGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99851118G>A , CM000663.2:g.99851118G>A GRCh38
NC_000001.10:g.100316674G>A , CM000663.1:g.100316674G>A GRCh37
NC_000001.9:g.100089262G>A NCBI36
NG_012865.1:g.6035G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361915.8:c.76G>A MANE Select ENSP00000355106.3:p.Glu26Lys
ENST00000294724.8:c.76G>A ENSP00000294724.4:p.Glu26Lys
ENST00000361302.7:c.-116G>A ENSP00000354971.3:n.-116G>A
ENST00000361915.7:c.76G>A ENSP00000355106.3:p.Glu26Lys
ENST00000370163.7:c.76G>A ENSP00000359182.3:p.Glu26Lys
ENST00000370165.7:c.76G>A ENSP00000359184.3:p.Glu26Lys
NM_000028.2:c.76G>A NP_000019.2:p.Glu26Lys
NM_000642.2:c.76G>A NP_000633.2:p.Glu26Lys
NM_000643.2:c.76G>A NP_000634.2:p.Glu26Lys
NM_000644.2:c.76G>A NP_000635.2:p.Glu26Lys
NM_000646.2:c.-116G>A NP_000637.2:n.-116G>A
XM_005270557.1:c.76G>A XP_005270614.1:p.Glu26Lys
XM_005270557.2:c.76G>A XP_005270614.1:p.Glu26Lys
NM_000642.3:c.76G>A MANE Select NP_000633.2:p.Glu26Lys