Canonical Allele Identifier: CA337834560
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1043863C>A , CM000663.2:g.1043863C>A GRCh38
NC_000001.10:g.979243C>A , CM000663.1:g.979243C>A GRCh37
NC_000001.9:g.969106C>A NCBI36
NG_016346.1:g.28741C>A , LRG_198:g.28741C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1839C>A MANE Select ENSP00000368678.2:p.Cys613Ter
ENST00000651234.1:c.1524C>A ENSP00000499046.1:p.Cys508Ter
ENST00000652369.1:c.1524C>A ENSP00000498543.1:p.Cys508Ter
ENST00000379370.6:c.1839C>A ENSP00000368678.2:p.Cys613Ter
ENST00000620552.4:c.1425C>A ENSP00000484607.1:p.Cys475Ter
NM_001305275.1:c.1839C>A NP_001292204.1:p.Cys613Ter
NM_198576.3:c.1839C>A NP_940978.2:p.Cys613Ter
XM_005244749.2:c.1839C>A XP_005244806.1:p.Cys613Ter
XM_006710635.2:c.1839C>A XP_006710698.1:p.Cys613Ter
XM_011541429.1:c.1839C>A XP_011539731.1:p.Cys613Ter
XM_011541430.1:c.966C>A XP_011539732.1:p.Cys322Ter
XM_011541431.1:c.105C>A XP_011539733.1:p.Cys35Ter
XR_946650.1:n.1906C>A
NM_001364727.1:c.1524C>A NP_001351656.1:p.Cys508Ter
XM_005244749.3:c.1839C>A XP_005244806.1:p.Cys613Ter
XM_011541429.2:c.1839C>A XP_011539731.1:p.Cys613Ter
XR_946650.2:n.1910C>A
NM_001305275.2:c.1839C>A NP_001292204.1:p.Cys613Ter
NM_198576.4:c.1839C>A MANE Select NP_940978.2:p.Cys613Ter
NM_001364727.2:c.1524C>A NP_001351656.1:p.Cys508Ter