Canonical Allele Identifier: CA1183924534

Gene: AGL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.99862402_99862404delinsCTT , CM000663.2:g.99862402_99862404delinsCTT	GRCh38
NC_000001.10:g.100327958_100327960delinsCTT , CM000663.1:g.100327958_100327960delinsCTT	GRCh37
NC_000001.9:g.100100546_100100548delinsCTT	NCBI36
NG_012865.1:g.17319_17321delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361915.8:c.439_441delinsCTT MANE Select	ENSP00000355106.3:p.Leu147=
ENST00000637337.1:n.650_652delinsCTT
ENST00000294724.8:c.439_441delinsCTT	ENSP00000294724.4:p.Leu147=
ENST00000361302.7:c.391_393delinsCTT	ENSP00000354971.3:p.Leu131=
ENST00000361522.4:c.388_390delinsCTT	ENSP00000354635.4:p.Leu130=
ENST00000361915.7:c.439_441delinsCTT	ENSP00000355106.3:p.Leu147=
ENST00000370161.6:c.391_393delinsCTT	ENSP00000359180.2:p.Leu131=
ENST00000370163.7:c.439_441delinsCTT	ENSP00000359182.3:p.Leu147=
ENST00000370165.7:c.439_441delinsCTT	ENSP00000359184.3:p.Leu147=
NM_000028.2:c.439_441delinsCTT	NP_000019.2:p.Leu147=
NM_000642.2:c.439_441delinsCTT	NP_000633.2:p.Leu147=
NM_000643.2:c.439_441delinsCTT	NP_000634.2:p.Leu147=
NM_000644.2:c.439_441delinsCTT	NP_000635.2:p.Leu147=
NM_000645.2:c.388_390delinsCTT	NP_000636.2:p.Leu130=
NM_000646.2:c.391_393delinsCTT	NP_000637.2:p.Leu131=
XM_005270557.1:c.439_441delinsCTT	XP_005270614.1:p.Leu147=
XM_005270557.2:c.439_441delinsCTT	XP_005270614.1:p.Leu147=
NM_000642.3:c.439_441delinsCTT MANE Select	NP_000633.2:p.Leu147=