Canonical Allele Identifier: CA2642491922

Gene: AGRN

Linked Data

• gnomAD v4: 1-1047696-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1047696T>A , CM000663.2:g.1047696T>A	GRCh38
NC_000001.10:g.983076T>A , CM000663.1:g.983076T>A	GRCh37
NC_000001.9:g.972939T>A	NCBI36
NG_016346.1:g.32574T>A , LRG_198:g.32574T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.3631+9T>A MANE Select	ENSP00000368678.2:n.3631+9T>A
ENST00000651234.1:c.3316+9T>A	ENSP00000499046.1:n.3316+9T>A
ENST00000652369.1:c.3316+9T>A	ENSP00000498543.1:n.3316+9T>A
ENST00000379370.6:c.3631+9T>A	ENSP00000368678.2:n.3631+9T>A
ENST00000466223.1:n.369+9T>A
ENST00000478677.1:n.213+9T>A
ENST00000620552.4:c.3217+9T>A	ENSP00000484607.1:n.3217+9T>A
NM_001305275.1:c.3631+9T>A	NP_001292204.1:n.3631+9T>A
NM_198576.3:c.3631+9T>A	NP_940978.2:n.3631+9T>A
XM_005244749.2:c.3631+9T>A	XP_005244806.1:n.3631+9T>A
XM_006710635.2:c.3631+9T>A	XP_006710698.1:n.3631+9T>A
XM_011541429.1:c.3631+9T>A	XP_011539731.1:n.3631+9T>A
XM_011541430.1:c.2758+9T>A	XP_011539732.1:n.2758+9T>A
XM_011541431.1:c.1897+9T>A	XP_011539733.1:n.1897+9T>A
XR_946650.1:n.3698+9T>A
NM_001364727.1:c.3316+9T>A	NP_001351656.1:n.3316+9T>A
XM_005244749.3:c.3631+9T>A	XP_005244806.1:n.3631+9T>A
XM_011541429.2:c.3631+9T>A	XP_011539731.1:n.3631+9T>A
XR_946650.2:n.3702+9T>A
NM_001305275.2:c.3631+9T>A	NP_001292204.1:n.3631+9T>A
NM_198576.4:c.3631+9T>A MANE Select	NP_940978.2:n.3631+9T>A
NM_001364727.2:c.3316+9T>A	NP_001351656.1:n.3316+9T>A