Canonical Allele Identifier: CA520620608
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs1233929956

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1050063_1050065del , CM000663.2:g.1050063_1050065del GRCh38
NC_000001.10:g.985443_985445del , CM000663.1:g.985443_985445del GRCh37
NC_000001.9:g.975306_975308del NCBI36
NG_016346.1:g.34941_34943del , LRG_198:g.34941_34943del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4879+26_4879+28del MANE Select ENSP00000368678.2:n.4879+26_4879+28del
ENST00000651234.1:c.4564+26_4564+28del ENSP00000499046.1:n.4564+26_4564+28del
ENST00000652369.1:c.4564+26_4564+28del ENSP00000498543.1:n.4564+26_4564+28del
ENST00000379370.6:c.4879+26_4879+28del ENSP00000368678.2:n.4879+26_4879+28del
ENST00000620552.4:c.4465+26_4465+28del ENSP00000484607.1:n.4465+26_4465+28del
NM_001305275.1:c.4879+26_4879+28del NP_001292204.1:n.4879+26_4879+28del
NM_198576.3:c.4879+26_4879+28del NP_940978.2:n.4879+26_4879+28del
XM_005244749.2:c.4879+26_4879+28del XP_005244806.1:n.4879+26_4879+28del
XM_006710635.2:c.4879+26_4879+28del XP_006710698.1:n.4879+26_4879+28del
XM_011541429.1:c.4879+26_4879+28del XP_011539731.1:n.4879+26_4879+28del
XM_011541430.1:c.4006+26_4006+28del XP_011539732.1:n.4006+26_4006+28del
XM_011541431.1:c.3145+26_3145+28del XP_011539733.1:n.3145+26_3145+28del
XR_946650.1:n.4946+26_4946+28del
NM_001364727.1:c.4564+26_4564+28del NP_001351656.1:n.4564+26_4564+28del
XM_005244749.3:c.4879+26_4879+28del XP_005244806.1:n.4879+26_4879+28del
XM_011541429.2:c.4879+26_4879+28del XP_011539731.1:n.4879+26_4879+28del
XR_946650.2:n.4950+26_4950+28del
NM_001305275.2:c.4879+26_4879+28del NP_001292204.1:n.4879+26_4879+28del
NM_198576.4:c.4879+26_4879+28del MANE Select NP_940978.2:n.4879+26_4879+28del
NM_001364727.2:c.4564+26_4564+28del NP_001351656.1:n.4564+26_4564+28del