Canonical Allele Identifier: CA1148773503
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs1645020706

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1044002del , CM000663.2:g.1044002del GRCh38
NC_000001.10:g.979382del , CM000663.1:g.979382del GRCh37
NC_000001.9:g.969245del NCBI36
NG_016346.1:g.28880del , LRG_198:g.28880del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1978del MANE Select ENSP00000368678.2:p.Arg660GlyfsTer?
ENST00000651234.1:c.1663del ENSP00000499046.1:p.Arg555GlyfsTer?
ENST00000652369.1:c.1663del ENSP00000498543.1:p.Arg555GlyfsTer?
ENST00000379370.6:c.1978del ENSP00000368678.2:p.Arg660GlyfsTer?
ENST00000620552.4:c.1564del ENSP00000484607.1:p.Arg522GlyfsTer?
NM_001305275.1:c.1978del NP_001292204.1:p.Arg660GlyfsTer?
NM_198576.3:c.1978del NP_940978.2:p.Arg660GlyfsTer?
XM_005244749.2:c.1978del XP_005244806.1:p.Arg660GlyfsTer?
XM_006710635.2:c.1978del XP_006710698.1:p.Arg660GlyfsTer?
XM_011541429.1:c.1978del XP_011539731.1:p.Arg660GlyfsTer?
XM_011541430.1:c.1105del XP_011539732.1:p.Arg369GlyfsTer?
XM_011541431.1:c.244del XP_011539733.1:p.Arg82GlyfsTer?
XR_946650.1:n.2045del
NM_001364727.1:c.1663del NP_001351656.1:p.Arg555GlyfsTer?
XM_005244749.3:c.1978del XP_005244806.1:p.Arg660GlyfsTer?
XM_011541429.2:c.1978del XP_011539731.1:p.Arg660GlyfsTer?
XR_946650.2:n.2049del
NM_001305275.2:c.1978del NP_001292204.1:p.Arg660GlyfsTer?
NM_198576.4:c.1978del MANE Select NP_940978.2:p.Arg660GlyfsTer?
NM_001364727.2:c.1663del NP_001351656.1:p.Arg555GlyfsTer?