Canonical Allele Identifier: CA2642491937
Gene: AGRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047759_1047760del , CM000663.2:g.1047759_1047760del GRCh38
NC_000001.10:g.983139_983140del , CM000663.1:g.983139_983140del GRCh37
NC_000001.9:g.973002_973003del NCBI36
NG_016346.1:g.32637_32638del , LRG_198:g.32637_32638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3632-17_3632-16del MANE Select ENSP00000368678.2:n.3632-17_3632-16del
ENST00000651234.1:c.3317-17_3317-16del ENSP00000499046.1:n.3317-17_3317-16del
ENST00000652369.1:c.3317-17_3317-16del ENSP00000498543.1:n.3317-17_3317-16del
ENST00000379370.6:c.3632-17_3632-16del ENSP00000368678.2:n.3632-17_3632-16del
ENST00000466223.1:n.370-17_370-16del
ENST00000478677.1:n.214-17_214-16del
ENST00000620552.4:c.3218-17_3218-16del ENSP00000484607.1:n.3218-17_3218-16del
NM_001305275.1:c.3632-17_3632-16del NP_001292204.1:n.3632-17_3632-16del
NM_198576.3:c.3632-17_3632-16del NP_940978.2:n.3632-17_3632-16del
XM_005244749.2:c.3632-17_3632-16del XP_005244806.1:n.3632-17_3632-16del
XM_006710635.2:c.3632-17_3632-16del XP_006710698.1:n.3632-17_3632-16del
XM_011541429.1:c.3632-17_3632-16del XP_011539731.1:n.3632-17_3632-16del
XM_011541430.1:c.2759-17_2759-16del XP_011539732.1:n.2759-17_2759-16del
XM_011541431.1:c.1898-17_1898-16del XP_011539733.1:n.1898-17_1898-16del
XR_946650.1:n.3699-17_3699-16del
NM_001364727.1:c.3317-17_3317-16del NP_001351656.1:n.3317-17_3317-16del
XM_005244749.3:c.3632-17_3632-16del XP_005244806.1:n.3632-17_3632-16del
XM_011541429.2:c.3632-17_3632-16del XP_011539731.1:n.3632-17_3632-16del
XR_946650.2:n.3703-17_3703-16del
NM_001305275.2:c.3632-17_3632-16del NP_001292204.1:n.3632-17_3632-16del
NM_198576.4:c.3632-17_3632-16del MANE Select NP_940978.2:n.3632-17_3632-16del
NM_001364727.2:c.3317-17_3317-16del NP_001351656.1:n.3317-17_3317-16del