Canonical Allele Identifier: CA2574258706

Gene: AGRN

Linked Data

• gnomAD v4: 1-1048122-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1048126del , CM000663.2:g.1048126del	GRCh38
NC_000001.10:g.983506del , CM000663.1:g.983506del	GRCh37
NC_000001.9:g.973369del	NCBI36
NG_016346.1:g.33004del , LRG_198:g.33004del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3866del MANE Select	ENSP00000368678.2:p.Pro1289ArgfsTer?
ENST00000651234.1:c.3551del	ENSP00000499046.1:p.Pro1184ArgfsTer?
ENST00000652369.1:c.3551del	ENSP00000498543.1:p.Pro1184ArgfsTer?
ENST00000379370.6:c.3866del	ENSP00000368678.2:p.Pro1289ArgfsTer?
ENST00000620552.4:c.3452del	ENSP00000484607.1:p.Pro1151ArgfsTer?
NM_001305275.1:c.3866del	NP_001292204.1:p.Pro1289ArgfsTer?
NM_198576.3:c.3866del	NP_940978.2:p.Pro1289ArgfsTer?
XM_005244749.2:c.3866del	XP_005244806.1:p.Pro1289ArgfsTer?
XM_006710635.2:c.3866del	XP_006710698.1:p.Pro1289ArgfsTer?
XM_011541429.1:c.3866del	XP_011539731.1:p.Pro1289ArgfsTer?
XM_011541430.1:c.2993del	XP_011539732.1:p.Pro998ArgfsTer?
XM_011541431.1:c.2132del	XP_011539733.1:p.Pro711ArgfsTer?
XR_946650.1:n.3933del
NM_001364727.1:c.3551del	NP_001351656.1:p.Pro1184ArgfsTer?
XM_005244749.3:c.3866del	XP_005244806.1:p.Pro1289ArgfsTer?
XM_011541429.2:c.3866del	XP_011539731.1:p.Pro1289ArgfsTer?
XR_946650.2:n.3937del
NM_001305275.2:c.3866del	NP_001292204.1:p.Pro1289ArgfsTer?
NM_198576.4:c.3866del MANE Select	NP_940978.2:p.Pro1289ArgfsTer?
NM_001364727.2:c.3551del	NP_001351656.1:p.Pro1184ArgfsTer?