Canonical Allele Identifier: CA2642490967
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1044090_1044091del , CM000663.2:g.1044090_1044091del GRCh38
NC_000001.10:g.979470_979471del , CM000663.1:g.979470_979471del GRCh37
NC_000001.9:g.969333_969334del NCBI36
NG_016346.1:g.28968_28969del , LRG_198:g.28968_28969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.2000-19_2000-18del MANE Select ENSP00000368678.2:n.2000-19_2000-18del
ENST00000651234.1:c.1685-19_1685-18del ENSP00000499046.1:n.1685-19_1685-18del
ENST00000652369.1:c.1685-19_1685-18del ENSP00000498543.1:n.1685-19_1685-18del
ENST00000379370.6:c.2000-19_2000-18del ENSP00000368678.2:n.2000-19_2000-18del
ENST00000620552.4:c.1586-19_1586-18del ENSP00000484607.1:n.1586-19_1586-18del
NM_001305275.1:c.2000-19_2000-18del NP_001292204.1:n.2000-19_2000-18del
NM_198576.3:c.2000-19_2000-18del NP_940978.2:n.2000-19_2000-18del
XM_005244749.2:c.2000-19_2000-18del XP_005244806.1:n.2000-19_2000-18del
XM_006710635.2:c.2000-19_2000-18del XP_006710698.1:n.2000-19_2000-18del
XM_011541429.1:c.2000-19_2000-18del XP_011539731.1:n.2000-19_2000-18del
XM_011541430.1:c.1127-19_1127-18del XP_011539732.1:n.1127-19_1127-18del
XM_011541431.1:c.266-19_266-18del XP_011539733.1:n.266-19_266-18del
XR_946650.1:n.2067-19_2067-18del
NM_001364727.1:c.1685-19_1685-18del NP_001351656.1:n.1685-19_1685-18del
XM_005244749.3:c.2000-19_2000-18del XP_005244806.1:n.2000-19_2000-18del
XM_011541429.2:c.2000-19_2000-18del XP_011539731.1:n.2000-19_2000-18del
XR_946650.2:n.2071-19_2071-18del
NM_001305275.2:c.2000-19_2000-18del NP_001292204.1:n.2000-19_2000-18del
NM_198576.4:c.2000-19_2000-18del MANE Select NP_940978.2:n.2000-19_2000-18del
NM_001364727.2:c.1685-19_1685-18del NP_001351656.1:n.1685-19_1685-18del