Canonical Allele Identifier: CA997654956
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs1645155345

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1048141_1048142del , CM000663.2:g.1048141_1048142del GRCh38
NC_000001.10:g.983521_983522del , CM000663.1:g.983521_983522del GRCh37
NC_000001.9:g.973384_973385del NCBI36
NG_016346.1:g.33019_33020del , LRG_198:g.33019_33020del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3881_3882del MANE Select ENSP00000368678.2:p.Thr1294LysfsTer?
ENST00000651234.1:c.3566_3567del ENSP00000499046.1:p.Thr1189LysfsTer?
ENST00000652369.1:c.3566_3567del ENSP00000498543.1:p.Thr1189LysfsTer?
ENST00000379370.6:c.3881_3882del ENSP00000368678.2:p.Thr1294LysfsTer?
ENST00000620552.4:c.3467_3468del ENSP00000484607.1:p.Thr1156LysfsTer?
NM_001305275.1:c.3881_3882del NP_001292204.1:p.Thr1294LysfsTer?
NM_198576.3:c.3881_3882del NP_940978.2:p.Thr1294LysfsTer?
XM_005244749.2:c.3881_3882del XP_005244806.1:p.Thr1294LysfsTer?
XM_006710635.2:c.3881_3882del XP_006710698.1:p.Thr1294LysfsTer?
XM_011541429.1:c.3881_3882del XP_011539731.1:p.Thr1294LysfsTer?
XM_011541430.1:c.3008_3009del XP_011539732.1:p.Thr1003LysfsTer?
XM_011541431.1:c.2147_2148del XP_011539733.1:p.Thr716LysfsTer?
XR_946650.1:n.3948_3949del
NM_001364727.1:c.3566_3567del NP_001351656.1:p.Thr1189LysfsTer?
XM_005244749.3:c.3881_3882del XP_005244806.1:p.Thr1294LysfsTer?
XM_011541429.2:c.3881_3882del XP_011539731.1:p.Thr1294LysfsTer?
XR_946650.2:n.3952_3953del
NM_001305275.2:c.3881_3882del NP_001292204.1:p.Thr1294LysfsTer?
NM_198576.4:c.3881_3882del MANE Select NP_940978.2:p.Thr1294LysfsTer?
NM_001364727.2:c.3566_3567del NP_001351656.1:p.Thr1189LysfsTer?