Canonical Allele Identifier: CA1141874301
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1043808C= , CM000663.2:g.1043808C= GRCh38
NC_000001.10:g.979188C= , CM000663.1:g.979188C= GRCh37
NC_000001.9:g.969051C= NCBI36
NG_016346.1:g.28686C= , LRG_198:g.28686C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1799-15C= MANE Select ENSP00000368678.2:n.1799-15C=
ENST00000651234.1:c.1484-15C= ENSP00000499046.1:n.1484-15C=
ENST00000652369.1:c.1484-15C= ENSP00000498543.1:n.1484-15C=
ENST00000379370.6:c.1799-15C= ENSP00000368678.2:n.1799-15C=
ENST00000620552.4:c.1385-15C= ENSP00000484607.1:n.1385-15C=
NM_001305275.1:c.1799-15C= NP_001292204.1:n.1799-15C=
NM_198576.3:c.1799-15C= NP_940978.2:n.1799-15C=
XM_005244749.2:c.1799-15C= XP_005244806.1:n.1799-15C=
XM_006710635.2:c.1799-15C= XP_006710698.1:n.1799-15C=
XM_011541429.1:c.1799-15C= XP_011539731.1:n.1799-15C=
XM_011541430.1:c.926-15C= XP_011539732.1:n.926-15C=
XM_011541431.1:c.65-15C= XP_011539733.1:n.65-15C=
XR_946650.1:n.1866-15C=
NM_001364727.1:c.1484-15C= NP_001351656.1:n.1484-15C=
XM_005244749.3:c.1799-15C= XP_005244806.1:n.1799-15C=
XM_011541429.2:c.1799-15C= XP_011539731.1:n.1799-15C=
XR_946650.2:n.1870-15C=
NM_001305275.2:c.1799-15C= NP_001292204.1:n.1799-15C=
NM_198576.4:c.1799-15C= MANE Select NP_940978.2:n.1799-15C=
NM_001364727.2:c.1484-15C= NP_001351656.1:n.1484-15C=