Canonical Allele Identifier: CA1148805646
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1048306T= , CM000663.2:g.1048306T= GRCh38
NC_000001.10:g.983686T= , CM000663.1:g.983686T= GRCh37
NC_000001.9:g.973549T= NCBI36
NG_016346.1:g.33184T= , LRG_198:g.33184T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4046T= MANE Select ENSP00000368678.2:p.Leu1349=
ENST00000651234.1:c.3731T= ENSP00000499046.1:p.Leu1244=
ENST00000652369.1:c.3731T= ENSP00000498543.1:p.Leu1244=
ENST00000379370.6:c.4046T= ENSP00000368678.2:p.Leu1349=
ENST00000620552.4:c.3632T= ENSP00000484607.1:p.Leu1211=
NM_001305275.1:c.4046T= NP_001292204.1:p.Leu1349=
NM_198576.3:c.4046T= NP_940978.2:p.Leu1349=
XM_005244749.2:c.4046T= XP_005244806.1:p.Leu1349=
XM_006710635.2:c.4046T= XP_006710698.1:p.Leu1349=
XM_011541429.1:c.4046T= XP_011539731.1:p.Leu1349=
XM_011541430.1:c.3173T= XP_011539732.1:p.Leu1058=
XM_011541431.1:c.2312T= XP_011539733.1:p.Leu771=
XR_946650.1:n.4113T=
NM_001364727.1:c.3731T= NP_001351656.1:p.Leu1244=
XM_005244749.3:c.4046T= XP_005244806.1:p.Leu1349=
XM_011541429.2:c.4046T= XP_011539731.1:p.Leu1349=
XR_946650.2:n.4117T=
NM_001305275.2:c.4046T= NP_001292204.1:p.Leu1349=
NM_198576.4:c.4046T= MANE Select NP_940978.2:p.Leu1349=
NM_001364727.2:c.3731T= NP_001351656.1:p.Leu1244=