Canonical Allele Identifier: CA1148749366

Gene: AGRN

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1050172_1050189delinsTGGCATGGGGTGCAGGAG , CM000663.2:g.1050172_1050189delinsTGGCATGGGGTGCAGGAG	GRCh38
NC_000001.10:g.985552_985569delinsTGGCATGGGGTGCAGGAG , CM000663.1:g.985552_985569delinsTGGCATGGGGTGCAGGAG	GRCh37
NC_000001.9:g.975415_975432delinsTGGCATGGGGTGCAGGAG	NCBI36
NG_016346.1:g.35050_35067delinsTGGCATGGGGTGCAGGAG , LRG_198:g.35050_35067delinsTGGCATGGGGTGCAGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG MANE Select	ENSP00000368678.2:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
ENST00000651234.1:c.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG	ENSP00000499046.1:n.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG
ENST00000652369.1:c.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG	ENSP00000498543.1:n.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG
ENST00000379370.6:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	ENSP00000368678.2:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
ENST00000620552.4:c.4466-61_4466-44delinsTGGCATGGGGTGCAGGAG	ENSP00000484607.1:n.4466-61_4466-44delinsTGGCATGGGGTGCAGGAG
NM_001305275.1:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	NP_001292204.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
NM_198576.3:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	NP_940978.2:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
XM_005244749.2:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	XP_005244806.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
XM_006710635.2:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	XP_006710698.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
XM_011541429.1:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	XP_011539731.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
XM_011541430.1:c.4007-61_4007-44delinsTGGCATGGGGTGCAGGAG	XP_011539732.1:n.4007-61_4007-44delinsTGGCATGGGGTGCAGGAG
XM_011541431.1:c.3146-61_3146-44delinsTGGCATGGGGTGCAGGAG	XP_011539733.1:n.3146-61_3146-44delinsTGGCATGGGGTGCAGGAG
XR_946650.1:n.4947-61_4947-44delinsTGGCATGGGGTGCAGGAG
NM_001364727.1:c.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG	NP_001351656.1:n.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG
XM_005244749.3:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	XP_005244806.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
XM_011541429.2:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	XP_011539731.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
XR_946650.2:n.4951-61_4951-44delinsTGGCATGGGGTGCAGGAG
NM_001305275.2:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG	NP_001292204.1:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
NM_198576.4:c.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG MANE Select	NP_940978.2:n.4880-61_4880-44delinsTGGCATGGGGTGCAGGAG
NM_001364727.2:c.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG	NP_001351656.1:n.4565-61_4565-44delinsTGGCATGGGGTGCAGGAG