Canonical Allele Identifier: CA2642487509

Gene: AGRN

Linked Data

• gnomAD v4: 1-1022143-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1022143C>A , CM000663.2:g.1022143C>A	GRCh38
NC_000001.10:g.957523C>A , CM000663.1:g.957523C>A	GRCh37
NC_000001.9:g.947386C>A	NCBI36
NG_016346.1:g.7021C>A , LRG_198:g.7021C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.202-58C>A MANE Select	ENSP00000368678.2:n.202-58C>A
ENST00000379370.6:c.202-58C>A	ENSP00000368678.2:n.202-58C>A
ENST00000620552.4:c.-213-58C>A	ENSP00000484607.1:n.-213-58C>A
NM_001305275.1:c.202-58C>A	NP_001292204.1:n.202-58C>A
NM_198576.3:c.202-58C>A	NP_940978.2:n.202-58C>A
XM_005244749.2:c.202-58C>A	XP_005244806.1:n.202-58C>A
XM_006710635.2:c.202-58C>A	XP_006710698.1:n.202-58C>A
XM_011541429.1:c.202-58C>A	XP_011539731.1:n.202-58C>A
XM_011541430.1:c.202-58C>A	XP_011539732.1:n.202-58C>A
XR_946650.1:n.269-58C>A
XM_005244749.3:c.202-58C>A	XP_005244806.1:n.202-58C>A
XM_011541429.2:c.202-58C>A	XP_011539731.1:n.202-58C>A
XR_946650.2:n.273-58C>A
NM_001305275.2:c.202-58C>A	NP_001292204.1:n.202-58C>A
NM_198576.4:c.202-58C>A MANE Select	NP_940978.2:n.202-58C>A