Canonical Allele Identifier: CA2642492072
Gene: AGRN HGNC NCBI

Linked Data

gnomAD v4: 1-1050067-G-GA

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1050067_1050068insA , CM000663.2:g.1050067_1050068insA GRCh38
NC_000001.10:g.985447_985448insA , CM000663.1:g.985447_985448insA GRCh37
NC_000001.9:g.975310_975311insA NCBI36
NG_016346.1:g.34945_34946insA , LRG_198:g.34945_34946insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4879+30_4879+31insA MANE Select ENSP00000368678.2:n.4879+30_4879+31insA
ENST00000651234.1:c.4564+30_4564+31insA ENSP00000499046.1:n.4564+30_4564+31insA
ENST00000652369.1:c.4564+30_4564+31insA ENSP00000498543.1:n.4564+30_4564+31insA
ENST00000379370.6:c.4879+30_4879+31insA ENSP00000368678.2:n.4879+30_4879+31insA
ENST00000620552.4:c.4465+30_4465+31insA ENSP00000484607.1:n.4465+30_4465+31insA
NM_001305275.1:c.4879+30_4879+31insA NP_001292204.1:n.4879+30_4879+31insA
NM_198576.3:c.4879+30_4879+31insA NP_940978.2:n.4879+30_4879+31insA
XM_005244749.2:c.4879+30_4879+31insA XP_005244806.1:n.4879+30_4879+31insA
XM_006710635.2:c.4879+30_4879+31insA XP_006710698.1:n.4879+30_4879+31insA
XM_011541429.1:c.4879+30_4879+31insA XP_011539731.1:n.4879+30_4879+31insA
XM_011541430.1:c.4006+30_4006+31insA XP_011539732.1:n.4006+30_4006+31insA
XM_011541431.1:c.3145+30_3145+31insA XP_011539733.1:n.3145+30_3145+31insA
XR_946650.1:n.4946+30_4946+31insA
NM_001364727.1:c.4564+30_4564+31insA NP_001351656.1:n.4564+30_4564+31insA
XM_005244749.3:c.4879+30_4879+31insA XP_005244806.1:n.4879+30_4879+31insA
XM_011541429.2:c.4879+30_4879+31insA XP_011539731.1:n.4879+30_4879+31insA
XR_946650.2:n.4950+30_4950+31insA
NM_001305275.2:c.4879+30_4879+31insA NP_001292204.1:n.4879+30_4879+31insA
NM_198576.4:c.4879+30_4879+31insA MANE Select NP_940978.2:n.4879+30_4879+31insA
NM_001364727.2:c.4564+30_4564+31insA NP_001351656.1:n.4564+30_4564+31insA