Canonical Allele Identifier: CA10584064
Gene: AGRN HGNC NCBI

Linked Data

ClinVar Variation Id: 243038
ClinVar RCV Id: RCV000235036
dbSNP Id: rs879253788

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1042140dup , CM000663.2:g.1042140dup GRCh38
NC_000001.10:g.977520dup , CM000663.1:g.977520dup GRCh37
NC_000001.9:g.967383dup NCBI36
NG_016346.1:g.27018dup , LRG_198:g.27018dup

Transcript Alleles

HGVS Amino-acid change
ENST00000379370.7:c.1362dup MANE Select ENSP00000368678.2:p.Ser455GlnfsTer8
ENST00000651234.1:c.1047dup ENSP00000499046.1:p.Ser350GlnfsTer8
ENST00000652369.1:c.1047dup ENSP00000498543.1:p.Ser350GlnfsTer8
ENST00000379370.6:c.1362dup ENSP00000368678.2:p.Ser455GlnfsTer8
ENST00000620552.4:c.948dup ENSP00000484607.1:p.Ser317GlnfsTer8
NM_001305275.1:c.1362dup NP_001292204.1:p.Ser455GlnfsTer8
NM_198576.3:c.1362dup NP_940978.2:p.Ser455GlnfsTer8
XM_005244749.2:c.1362dup XP_005244806.1:p.Ser455GlnfsTer8
XM_006710635.2:c.1362dup XP_006710698.1:p.Ser455GlnfsTer8
XM_011541429.1:c.1362dup XP_011539731.1:p.Ser455GlnfsTer8
XM_011541430.1:c.512-1099dup XP_011539732.1:n.512-1099dup
XR_946650.1:n.1429dup
NM_001364727.1:c.1047dup NP_001351656.1:p.Ser350GlnfsTer8
XM_005244749.3:c.1362dup XP_005244806.1:p.Ser455GlnfsTer8
XM_011541429.2:c.1362dup XP_011539731.1:p.Ser455GlnfsTer8
XR_946650.2:n.1433dup
NM_001305275.2:c.1362dup NP_001292204.1:p.Ser455GlnfsTer8
NM_198576.4:c.1362dup MANE Select NP_940978.2:p.Ser455GlnfsTer8
NM_001364727.2:c.1047dup NP_001351656.1:p.Ser350GlnfsTer8