Canonical Allele Identifier: CA1183927337
Gene: AGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.99876555_99876556delinsTG , CM000663.2:g.99876555_99876556delinsTG GRCh38
NC_000001.10:g.100342111_100342112delinsTG , CM000663.1:g.100342111_100342112delinsTG GRCh37
NC_000001.9:g.100114699_100114700delinsTG NCBI36
NG_012865.1:g.31472_31473delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361915.8:c.1381_1382delinsTG MANE Select ENSP00000355106.3:p.Trp461=
ENST00000637337.1:n.1592_1593delinsTG
ENST00000294724.8:c.1381_1382delinsTG ENSP00000294724.4:p.Trp461=
ENST00000361302.7:c.1333_1334delinsTG ENSP00000354971.3:p.Trp445=
ENST00000361522.4:c.1330_1331delinsTG ENSP00000354635.4:p.Trp444=
ENST00000361915.7:c.1381_1382delinsTG ENSP00000355106.3:p.Trp461=
ENST00000370161.6:c.1333_1334delinsTG ENSP00000359180.2:p.Trp445=
ENST00000370163.7:c.1381_1382delinsTG ENSP00000359182.3:p.Trp461=
ENST00000370165.7:c.1381_1382delinsTG ENSP00000359184.3:p.Trp461=
ENST00000477753.1:n.640_641delinsTG
NM_000028.2:c.1381_1382delinsTG NP_000019.2:p.Trp461=
NM_000642.2:c.1381_1382delinsTG NP_000633.2:p.Trp461=
NM_000643.2:c.1381_1382delinsTG NP_000634.2:p.Trp461=
NM_000644.2:c.1381_1382delinsTG NP_000635.2:p.Trp461=
NM_000645.2:c.1330_1331delinsTG NP_000636.2:p.Trp444=
NM_000646.2:c.1333_1334delinsTG NP_000637.2:p.Trp445=
XM_005270557.1:c.1381_1382delinsTG XP_005270614.1:p.Trp461=
XM_005270557.2:c.1381_1382delinsTG XP_005270614.1:p.Trp461=
NM_000642.3:c.1381_1382delinsTG MANE Select NP_000633.2:p.Trp461=