Canonical Allele Identifier: CA1148805294
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1048274C= , CM000663.2:g.1048274C= GRCh38
NC_000001.10:g.983654C= , CM000663.1:g.983654C= GRCh37
NC_000001.9:g.973517C= NCBI36
NG_016346.1:g.33152C= , LRG_198:g.33152C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4014C= MANE Select ENSP00000368678.2:p.Cys1338=
ENST00000651234.1:c.3699C= ENSP00000499046.1:p.Cys1233=
ENST00000652369.1:c.3699C= ENSP00000498543.1:p.Cys1233=
ENST00000379370.6:c.4014C= ENSP00000368678.2:p.Cys1338=
ENST00000620552.4:c.3600C= ENSP00000484607.1:p.Cys1200=
NM_001305275.1:c.4014C= NP_001292204.1:p.Cys1338=
NM_198576.3:c.4014C= NP_940978.2:p.Cys1338=
XM_005244749.2:c.4014C= XP_005244806.1:p.Cys1338=
XM_006710635.2:c.4014C= XP_006710698.1:p.Cys1338=
XM_011541429.1:c.4014C= XP_011539731.1:p.Cys1338=
XM_011541430.1:c.3141C= XP_011539732.1:p.Cys1047=
XM_011541431.1:c.2280C= XP_011539733.1:p.Cys760=
XR_946650.1:n.4081C=
NM_001364727.1:c.3699C= NP_001351656.1:p.Cys1233=
XM_005244749.3:c.4014C= XP_005244806.1:p.Cys1338=
XM_011541429.2:c.4014C= XP_011539731.1:p.Cys1338=
XR_946650.2:n.4085C=
NM_001305275.2:c.4014C= NP_001292204.1:p.Cys1338=
NM_198576.4:c.4014C= MANE Select NP_940978.2:p.Cys1338=
NM_001364727.2:c.3699C= NP_001351656.1:p.Cys1233=