Canonical Allele Identifier: CA1183941649
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99916636A= , CM000663.2:g.99916636A= GRCh38
NC_000001.10:g.100382192A= , CM000663.1:g.100382192A= GRCh37
NC_000001.9:g.100154780A= NCBI36
NG_012865.1:g.71553A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.4386A= MANE Select ENSP00000355106.3:p.Lys1462=
ENST00000637337.1:n.4597A=
ENST00000294724.8:c.4386A= ENSP00000294724.4:p.Lys1462=
ENST00000361302.7:c.4338A= ENSP00000354971.3:p.Lys1446=
ENST00000361522.4:c.4335A= ENSP00000354635.4:p.Lys1445=
ENST00000361915.7:c.4386A= ENSP00000355106.3:p.Lys1462=
ENST00000370161.6:c.4338A= ENSP00000359180.2:p.Lys1446=
ENST00000370163.7:c.4386A= ENSP00000359182.3:p.Lys1462=
ENST00000370165.7:c.4386A= ENSP00000359184.3:p.Lys1462=
NM_000028.2:c.4386A= NP_000019.2:p.Lys1462=
NM_000642.2:c.4386A= NP_000633.2:p.Lys1462=
NM_000643.2:c.4386A= NP_000634.2:p.Lys1462=
NM_000644.2:c.4386A= NP_000635.2:p.Lys1462=
NM_000645.2:c.4335A= NP_000636.2:p.Lys1445=
NM_000646.2:c.4338A= NP_000637.2:p.Lys1446=
XM_005270557.1:c.4386A= XP_005270614.1:p.Lys1462=
XR_947626.1:n.1318-3419T=
XR_947627.1:n.1207-3419T=
XR_947628.1:n.1312-3419T=
XR_947630.1:n.1250-3419T=
XR_947632.1:n.1136-3419T=
XR_947633.1:n.1247-3419T=
XR_947634.1:n.661-3419T=
XR_947635.1:n.729-3419T=
XM_005270557.2:c.4386A= XP_005270614.1:p.Lys1462=
XM_017000501.2:c.2646A= XP_016855990.1:p.Lys882=
NM_000642.3:c.4386A= MANE Select NP_000633.2:p.Lys1462=