Canonical Allele Identifier: CA1143833067
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1048127G= , CM000663.2:g.1048127G= GRCh38
NC_000001.10:g.983507G= , CM000663.1:g.983507G= GRCh37
NC_000001.9:g.973370G= NCBI36
NG_016346.1:g.33005G= , LRG_198:g.33005G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3867G= MANE Select ENSP00000368678.2:p.Pro1289=
ENST00000651234.1:c.3552G= ENSP00000499046.1:p.Pro1184=
ENST00000652369.1:c.3552G= ENSP00000498543.1:p.Pro1184=
ENST00000379370.6:c.3867G= ENSP00000368678.2:p.Pro1289=
ENST00000620552.4:c.3453G= ENSP00000484607.1:p.Pro1151=
NM_001305275.1:c.3867G= NP_001292204.1:p.Pro1289=
NM_198576.3:c.3867G= NP_940978.2:p.Pro1289=
XM_005244749.2:c.3867G= XP_005244806.1:p.Pro1289=
XM_006710635.2:c.3867G= XP_006710698.1:p.Pro1289=
XM_011541429.1:c.3867G= XP_011539731.1:p.Pro1289=
XM_011541430.1:c.2994G= XP_011539732.1:p.Pro998=
XM_011541431.1:c.2133G= XP_011539733.1:p.Pro711=
XR_946650.1:n.3934G=
NM_001364727.1:c.3552G= NP_001351656.1:p.Pro1184=
XM_005244749.3:c.3867G= XP_005244806.1:p.Pro1289=
XM_011541429.2:c.3867G= XP_011539731.1:p.Pro1289=
XR_946650.2:n.3938G=
NM_001305275.2:c.3867G= NP_001292204.1:p.Pro1289=
NM_198576.4:c.3867G= MANE Select NP_940978.2:p.Pro1289=
NM_001364727.2:c.3552G= NP_001351656.1:p.Pro1184=