Canonical Allele Identifier: CA1148772340
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1043874A= , CM000663.2:g.1043874A= GRCh38
NC_000001.10:g.979254A= , CM000663.1:g.979254A= GRCh37
NC_000001.9:g.969117A= NCBI36
NG_016346.1:g.28752A= , LRG_198:g.28752A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1850A= MANE Select ENSP00000368678.2:p.Gln617=
ENST00000651234.1:c.1535A= ENSP00000499046.1:p.Gln512=
ENST00000652369.1:c.1535A= ENSP00000498543.1:p.Gln512=
ENST00000379370.6:c.1850A= ENSP00000368678.2:p.Gln617=
ENST00000620552.4:c.1436A= ENSP00000484607.1:p.Gln479=
NM_001305275.1:c.1850A= NP_001292204.1:p.Gln617=
NM_198576.3:c.1850A= NP_940978.2:p.Gln617=
XM_005244749.2:c.1850A= XP_005244806.1:p.Gln617=
XM_006710635.2:c.1850A= XP_006710698.1:p.Gln617=
XM_011541429.1:c.1850A= XP_011539731.1:p.Gln617=
XM_011541430.1:c.977A= XP_011539732.1:p.Gln326=
XM_011541431.1:c.116A= XP_011539733.1:p.Gln39=
XR_946650.1:n.1917A=
NM_001364727.1:c.1535A= NP_001351656.1:p.Gln512=
XM_005244749.3:c.1850A= XP_005244806.1:p.Gln617=
XM_011541429.2:c.1850A= XP_011539731.1:p.Gln617=
XR_946650.2:n.1921A=
NM_001305275.2:c.1850A= NP_001292204.1:p.Gln617=
NM_198576.4:c.1850A= MANE Select NP_940978.2:p.Gln617=
NM_001364727.2:c.1535A= NP_001351656.1:p.Gln512=