Canonical Allele Identifier: CA1148745181
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1049698G= , CM000663.2:g.1049698G= GRCh38
NC_000001.10:g.985078G= , CM000663.1:g.985078G= GRCh37
NC_000001.9:g.974941G= NCBI36
NG_016346.1:g.34576G= , LRG_198:g.34576G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4647G= MANE Select ENSP00000368678.2:p.Gly1549=
ENST00000651234.1:c.4332G= ENSP00000499046.1:p.Gly1444=
ENST00000652369.1:c.4332G= ENSP00000498543.1:p.Gly1444=
ENST00000379370.6:c.4647G= ENSP00000368678.2:p.Gly1549=
ENST00000620552.4:c.4233G= ENSP00000484607.1:p.Gly1411=
NM_001305275.1:c.4647G= NP_001292204.1:p.Gly1549=
NM_198576.3:c.4647G= NP_940978.2:p.Gly1549=
XM_005244749.2:c.4647G= XP_005244806.1:p.Gly1549=
XM_006710635.2:c.4647G= XP_006710698.1:p.Gly1549=
XM_011541429.1:c.4647G= XP_011539731.1:p.Gly1549=
XM_011541430.1:c.3774G= XP_011539732.1:p.Gly1258=
XM_011541431.1:c.2913G= XP_011539733.1:p.Gly971=
XR_946650.1:n.4714G=
NM_001364727.1:c.4332G= NP_001351656.1:p.Gly1444=
XM_005244749.3:c.4647G= XP_005244806.1:p.Gly1549=
XM_011541429.2:c.4647G= XP_011539731.1:p.Gly1549=
XR_946650.2:n.4718G=
NM_001305275.2:c.4647G= NP_001292204.1:p.Gly1549=
NM_198576.4:c.4647G= MANE Select NP_940978.2:p.Gly1549=
NM_001364727.2:c.4332G= NP_001351656.1:p.Gly1444=