Canonical Allele Identifier: CA997657370

Gene: AGRN

Linked Data

• gnomAD v3: 1-1049743-C-CCGTGTGCTGCCCGAGGGTGGTG
• gnomAD v4: 1-1049743-C-CCGTGTGCTGCCCGAGGGTGGTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1049744_1049745insGTGTGCTGCCCGAGGGTGGTGC , CM000663.2:g.1049744_1049745insGTGTGCTGCCCGAGGGTGGTGC	GRCh38
NC_000001.10:g.985124_985125insGTGTGCTGCCCGAGGGTGGTGC , CM000663.1:g.985124_985125insGTGTGCTGCCCGAGGGTGGTGC	GRCh37
NC_000001.9:g.974987_974988insGTGTGCTGCCCGAGGGTGGTGC	NCBI36
NG_016346.1:g.34622_34623insGTGTGCTGCCCGAGGGTGGTGC , LRG_198:g.34622_34623insGTGTGCTGCCCGAGGGTGGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC MANE Select	ENSP00000368678.2:p.Gln1565ArgfsTer31
ENST00000651234.1:c.4378_4379insGTGTGCTGCCCGAGGGTGGTGC	ENSP00000499046.1:p.Gln1460ArgfsTer31
ENST00000652369.1:c.4378_4379insGTGTGCTGCCCGAGGGTGGTGC	ENSP00000498543.1:p.Gln1460ArgfsTer31
ENST00000379370.6:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	ENSP00000368678.2:p.Gln1565ArgfsTer31
ENST00000620552.4:c.4279_4280insGTGTGCTGCCCGAGGGTGGTGC	ENSP00000484607.1:p.Gln1427ArgfsTer31
NM_001305275.1:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	NP_001292204.1:p.Gln1565ArgfsTer31
NM_198576.3:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	NP_940978.2:p.Gln1565ArgfsTer31
XM_005244749.2:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	XP_005244806.1:p.Gln1565ArgfsTer31
XM_006710635.2:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	XP_006710698.1:p.Gln1565ArgfsTer31
XM_011541429.1:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	XP_011539731.1:p.Gln1565ArgfsTer31
XM_011541430.1:c.3820_3821insGTGTGCTGCCCGAGGGTGGTGC	XP_011539732.1:p.Gln1274ArgfsTer31
XM_011541431.1:c.2959_2960insGTGTGCTGCCCGAGGGTGGTGC	XP_011539733.1:p.Gln987ArgfsTer31
XR_946650.1:n.4760_4761insGTGTGCTGCCCGAGGGTGGTGC
NM_001364727.1:c.4378_4379insGTGTGCTGCCCGAGGGTGGTGC	NP_001351656.1:p.Gln1460ArgfsTer31
XM_005244749.3:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	XP_005244806.1:p.Gln1565ArgfsTer31
XM_011541429.2:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	XP_011539731.1:p.Gln1565ArgfsTer31
XR_946650.2:n.4764_4765insGTGTGCTGCCCGAGGGTGGTGC
NM_001305275.2:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC	NP_001292204.1:p.Gln1565ArgfsTer31
NM_198576.4:c.4693_4694insGTGTGCTGCCCGAGGGTGGTGC MANE Select	NP_940978.2:p.Gln1565ArgfsTer31
NM_001364727.2:c.4378_4379insGTGTGCTGCCCGAGGGTGGTGC	NP_001351656.1:p.Gln1460ArgfsTer31