Canonical Allele Identifier: CA1148804903

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048226_1048227delinsGC , CM000663.2:g.1048226_1048227delinsGC	GRCh38
NC_000001.10:g.983606_983607delinsGC , CM000663.1:g.983606_983607delinsGC	GRCh37
NC_000001.9:g.973469_973470delinsGC	NCBI36
NG_016346.1:g.33104_33105delinsGC , LRG_198:g.33104_33105delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3966_3967delinsGC MANE Select	ENSP00000368678.2:p.Arg1322=
ENST00000651234.1:c.3651_3652delinsGC	ENSP00000499046.1:p.Arg1217=
ENST00000652369.1:c.3651_3652delinsGC	ENSP00000498543.1:p.Arg1217=
ENST00000379370.6:c.3966_3967delinsGC	ENSP00000368678.2:p.Arg1322=
ENST00000620552.4:c.3552_3553delinsGC	ENSP00000484607.1:p.Arg1184=
NM_001305275.1:c.3966_3967delinsGC	NP_001292204.1:p.Arg1322=
NM_198576.3:c.3966_3967delinsGC	NP_940978.2:p.Arg1322=
XM_005244749.2:c.3966_3967delinsGC	XP_005244806.1:p.Arg1322=
XM_006710635.2:c.3966_3967delinsGC	XP_006710698.1:p.Arg1322=
XM_011541429.1:c.3966_3967delinsGC	XP_011539731.1:p.Arg1322=
XM_011541430.1:c.3093_3094delinsGC	XP_011539732.1:p.Arg1031=
XM_011541431.1:c.2232_2233delinsGC	XP_011539733.1:p.Arg744=
XR_946650.1:n.4033_4034delinsGC
NM_001364727.1:c.3651_3652delinsGC	NP_001351656.1:p.Arg1217=
XM_005244749.3:c.3966_3967delinsGC	XP_005244806.1:p.Arg1322=
XM_011541429.2:c.3966_3967delinsGC	XP_011539731.1:p.Arg1322=
XR_946650.2:n.4037_4038delinsGC
NM_001305275.2:c.3966_3967delinsGC	NP_001292204.1:p.Arg1322=
NM_198576.4:c.3966_3967delinsGC MANE Select	NP_940978.2:p.Arg1322=
NM_001364727.2:c.3651_3652delinsGC	NP_001351656.1:p.Arg1217=