Canonical Allele Identifier: CA2574221939
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1050205_1050210dup , CM000663.2:g.1050205_1050210dup GRCh38
NC_000001.10:g.985585_985590dup , CM000663.1:g.985585_985590dup GRCh37
NC_000001.9:g.975448_975453dup NCBI36
NG_016346.1:g.35083_35088dup , LRG_198:g.35083_35088dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4880-28_4880-23dup MANE Select ENSP00000368678.2:n.4880-28_4880-23dup
ENST00000651234.1:c.4565-28_4565-23dup ENSP00000499046.1:n.4565-28_4565-23dup
ENST00000652369.1:c.4565-28_4565-23dup ENSP00000498543.1:n.4565-28_4565-23dup
ENST00000379370.6:c.4880-28_4880-23dup ENSP00000368678.2:n.4880-28_4880-23dup
ENST00000620552.4:c.4466-28_4466-23dup ENSP00000484607.1:n.4466-28_4466-23dup
NM_001305275.1:c.4880-28_4880-23dup NP_001292204.1:n.4880-28_4880-23dup
NM_198576.3:c.4880-28_4880-23dup NP_940978.2:n.4880-28_4880-23dup
XM_005244749.2:c.4880-28_4880-23dup XP_005244806.1:n.4880-28_4880-23dup
XM_006710635.2:c.4880-28_4880-23dup XP_006710698.1:n.4880-28_4880-23dup
XM_011541429.1:c.4880-28_4880-23dup XP_011539731.1:n.4880-28_4880-23dup
XM_011541430.1:c.4007-28_4007-23dup XP_011539732.1:n.4007-28_4007-23dup
XM_011541431.1:c.3146-28_3146-23dup XP_011539733.1:n.3146-28_3146-23dup
XR_946650.1:n.4947-28_4947-23dup
NM_001364727.1:c.4565-28_4565-23dup NP_001351656.1:n.4565-28_4565-23dup
XM_005244749.3:c.4880-28_4880-23dup XP_005244806.1:n.4880-28_4880-23dup
XM_011541429.2:c.4880-28_4880-23dup XP_011539731.1:n.4880-28_4880-23dup
XR_946650.2:n.4951-28_4951-23dup
NM_001305275.2:c.4880-28_4880-23dup NP_001292204.1:n.4880-28_4880-23dup
NM_198576.4:c.4880-28_4880-23dup MANE Select NP_940978.2:n.4880-28_4880-23dup
NM_001364727.2:c.4565-28_4565-23dup NP_001351656.1:n.4565-28_4565-23dup