Canonical Allele Identifier: CA1183924460

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862356_99862357delinsAT , CM000663.2:g.99862356_99862357delinsAT	GRCh38
NC_000001.10:g.100327912_100327913delinsAT , CM000663.1:g.100327912_100327913delinsAT	GRCh37
NC_000001.9:g.100100500_100100501delinsAT	NCBI36
NG_012865.1:g.17273_17274delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.393_394delinsAT MANE Select	ENSP00000355106.3:p.Thr131=
ENST00000637337.1:n.604_605delinsAT
ENST00000294724.8:c.393_394delinsAT	ENSP00000294724.4:p.Thr131=
ENST00000361302.7:c.345_346delinsAT	ENSP00000354971.3:p.Thr115=
ENST00000361522.4:c.342_343delinsAT	ENSP00000354635.4:p.Thr114=
ENST00000361915.7:c.393_394delinsAT	ENSP00000355106.3:p.Thr131=
ENST00000370161.6:c.345_346delinsAT	ENSP00000359180.2:p.Thr115=
ENST00000370163.7:c.393_394delinsAT	ENSP00000359182.3:p.Thr131=
ENST00000370165.7:c.393_394delinsAT	ENSP00000359184.3:p.Thr131=
NM_000028.2:c.393_394delinsAT	NP_000019.2:p.Thr131=
NM_000642.2:c.393_394delinsAT	NP_000633.2:p.Thr131=
NM_000643.2:c.393_394delinsAT	NP_000634.2:p.Thr131=
NM_000644.2:c.393_394delinsAT	NP_000635.2:p.Thr131=
NM_000645.2:c.342_343delinsAT	NP_000636.2:p.Thr114=
NM_000646.2:c.345_346delinsAT	NP_000637.2:p.Thr115=
XM_005270557.1:c.393_394delinsAT	XP_005270614.1:p.Thr131=
XM_005270557.2:c.393_394delinsAT	XP_005270614.1:p.Thr131=
NM_000642.3:c.393_394delinsAT MANE Select	NP_000633.2:p.Thr131=