Canonical Allele Identifier: CA2742134930
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1049774del , CM000663.2:g.1049774del GRCh38
NC_000001.10:g.985154del , CM000663.1:g.985154del GRCh37
NC_000001.9:g.975017del NCBI36
NG_016346.1:g.34652del , LRG_198:g.34652del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4723del MANE Select ENSP00000368678.2:p.Gln1575SerfsTer?
ENST00000651234.1:c.4408del ENSP00000499046.1:p.Gln1470SerfsTer?
ENST00000652369.1:c.4408del ENSP00000498543.1:p.Gln1470SerfsTer?
ENST00000379370.6:c.4723del ENSP00000368678.2:p.Gln1575SerfsTer?
ENST00000620552.4:c.4309del ENSP00000484607.1:p.Gln1437SerfsTer?
NM_001305275.1:c.4723del NP_001292204.1:p.Gln1575SerfsTer?
NM_198576.3:c.4723del NP_940978.2:p.Gln1575SerfsTer?
XM_005244749.2:c.4723del XP_005244806.1:p.Gln1575SerfsTer?
XM_006710635.2:c.4723del XP_006710698.1:p.Gln1575SerfsTer?
XM_011541429.1:c.4723del XP_011539731.1:p.Gln1575SerfsTer?
XM_011541430.1:c.3850del XP_011539732.1:p.Gln1284SerfsTer?
XM_011541431.1:c.2989del XP_011539733.1:p.Gln997SerfsTer?
XR_946650.1:n.4790del
NM_001364727.1:c.4408del NP_001351656.1:p.Gln1470SerfsTer?
XM_005244749.3:c.4723del XP_005244806.1:p.Gln1575SerfsTer?
XM_011541429.2:c.4723del XP_011539731.1:p.Gln1575SerfsTer?
XR_946650.2:n.4794del
NM_001305275.2:c.4723del NP_001292204.1:p.Gln1575SerfsTer?
NM_198576.4:c.4723del MANE Select NP_940978.2:p.Gln1575SerfsTer?
NM_001364727.2:c.4408del NP_001351656.1:p.Gln1470SerfsTer?