Canonical Allele Identifier: CA337834291
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1043828T>A , CM000663.2:g.1043828T>A GRCh38
NC_000001.10:g.979208T>A , CM000663.1:g.979208T>A GRCh37
NC_000001.9:g.969071T>A NCBI36
NG_016346.1:g.28706T>A , LRG_198:g.28706T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1804T>A MANE Select ENSP00000368678.2:p.Cys602Ser
ENST00000651234.1:c.1489T>A ENSP00000499046.1:p.Cys497Ser
ENST00000652369.1:c.1489T>A ENSP00000498543.1:p.Cys497Ser
ENST00000379370.6:c.1804T>A ENSP00000368678.2:p.Cys602Ser
ENST00000620552.4:c.1390T>A ENSP00000484607.1:p.Cys464Ser
NM_001305275.1:c.1804T>A NP_001292204.1:p.Cys602Ser
NM_198576.3:c.1804T>A NP_940978.2:p.Cys602Ser
XM_005244749.2:c.1804T>A XP_005244806.1:p.Cys602Ser
XM_006710635.2:c.1804T>A XP_006710698.1:p.Cys602Ser
XM_011541429.1:c.1804T>A XP_011539731.1:p.Cys602Ser
XM_011541430.1:c.931T>A XP_011539732.1:p.Cys311Ser
XM_011541431.1:c.70T>A XP_011539733.1:p.Cys24Ser
XR_946650.1:n.1871T>A
NM_001364727.1:c.1489T>A NP_001351656.1:p.Cys497Ser
XM_005244749.3:c.1804T>A XP_005244806.1:p.Cys602Ser
XM_011541429.2:c.1804T>A XP_011539731.1:p.Cys602Ser
XR_946650.2:n.1875T>A
NM_001305275.2:c.1804T>A NP_001292204.1:p.Cys602Ser
NM_198576.4:c.1804T>A MANE Select NP_940978.2:p.Cys602Ser
NM_001364727.2:c.1489T>A NP_001351656.1:p.Cys497Ser