Canonical Allele Identifier: CA508020
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1041706_1041752del , CM000663.2:g.1041706_1041752del GRCh38
NC_000001.10:g.977086_977132del , CM000663.1:g.977086_977132del GRCh37
NC_000001.9:g.966949_966995del NCBI36
NG_016346.1:g.26584_26630del , LRG_198:g.26584_26630del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1177+4_1177+50del
ENST00000651234.1:c.862+4_862+50del
ENST00000652369.1:c.862+4_862+50del
ENST00000379370.6:c.1177+4_1177+50del
ENST00000620552.4:c.763+4_763+50del
NM_001305275.1:c.1177+4_1177+50del
NM_198576.3:c.1177+4_1177+50del
XM_005244749.2:c.1177+4_1177+50del
XM_006710635.2:c.1177+4_1177+50del
XM_011541429.1:c.1177+4_1177+50del
XM_011541430.1:c.512-1533_512-1487del XP_011539732.1:n.512-1533_512-1487del
XR_946650.1:n.1244+4_1244+50del
NM_001364727.1:c.862+4_862+50del
XM_005244749.3:c.1177+4_1177+50del
XM_011541429.2:c.1177+4_1177+50del
XR_946650.2:n.1248+4_1248+50del
NM_001305275.2:c.1177+4_1177+50del
NM_198576.4:c.1177+4_1177+50del
NM_001364727.2:c.862+4_862+50del