Canonical Allele Identifier: CA2574221938
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1050185_1050192del , CM000663.2:g.1050185_1050192del GRCh38
NC_000001.10:g.985565_985572del , CM000663.1:g.985565_985572del GRCh37
NC_000001.9:g.975428_975435del NCBI36
NG_016346.1:g.35063_35070del , LRG_198:g.35063_35070del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4880-48_4880-41del MANE Select ENSP00000368678.2:n.4880-48_4880-41del
ENST00000651234.1:c.4565-48_4565-41del ENSP00000499046.1:n.4565-48_4565-41del
ENST00000652369.1:c.4565-48_4565-41del ENSP00000498543.1:n.4565-48_4565-41del
ENST00000379370.6:c.4880-48_4880-41del ENSP00000368678.2:n.4880-48_4880-41del
ENST00000620552.4:c.4466-48_4466-41del ENSP00000484607.1:n.4466-48_4466-41del
NM_001305275.1:c.4880-48_4880-41del NP_001292204.1:n.4880-48_4880-41del
NM_198576.3:c.4880-48_4880-41del NP_940978.2:n.4880-48_4880-41del
XM_005244749.2:c.4880-48_4880-41del XP_005244806.1:n.4880-48_4880-41del
XM_006710635.2:c.4880-48_4880-41del XP_006710698.1:n.4880-48_4880-41del
XM_011541429.1:c.4880-48_4880-41del XP_011539731.1:n.4880-48_4880-41del
XM_011541430.1:c.4007-48_4007-41del XP_011539732.1:n.4007-48_4007-41del
XM_011541431.1:c.3146-48_3146-41del XP_011539733.1:n.3146-48_3146-41del
XR_946650.1:n.4947-48_4947-41del
NM_001364727.1:c.4565-48_4565-41del NP_001351656.1:n.4565-48_4565-41del
XM_005244749.3:c.4880-48_4880-41del XP_005244806.1:n.4880-48_4880-41del
XM_011541429.2:c.4880-48_4880-41del XP_011539731.1:n.4880-48_4880-41del
XR_946650.2:n.4951-48_4951-41del
NM_001305275.2:c.4880-48_4880-41del NP_001292204.1:n.4880-48_4880-41del
NM_198576.4:c.4880-48_4880-41del MANE Select NP_940978.2:n.4880-48_4880-41del
NM_001364727.2:c.4565-48_4565-41del NP_001351656.1:n.4565-48_4565-41del