Canonical Allele Identifier: CA2574351307
Gene: AGRN HGNC NCBI

Linked Data

gnomAD v4: 1-1043809-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1043809T>C , CM000663.2:g.1043809T>C GRCh38
NC_000001.10:g.979189T>C , CM000663.1:g.979189T>C GRCh37
NC_000001.9:g.969052T>C NCBI36
NG_016346.1:g.28687T>C , LRG_198:g.28687T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.1799-14T>C MANE Select ENSP00000368678.2:n.1799-14T>C
ENST00000651234.1:c.1484-14T>C ENSP00000499046.1:n.1484-14T>C
ENST00000652369.1:c.1484-14T>C ENSP00000498543.1:n.1484-14T>C
ENST00000379370.6:c.1799-14T>C ENSP00000368678.2:n.1799-14T>C
ENST00000620552.4:c.1385-14T>C ENSP00000484607.1:n.1385-14T>C
NM_001305275.1:c.1799-14T>C NP_001292204.1:n.1799-14T>C
NM_198576.3:c.1799-14T>C NP_940978.2:n.1799-14T>C
XM_005244749.2:c.1799-14T>C XP_005244806.1:n.1799-14T>C
XM_006710635.2:c.1799-14T>C XP_006710698.1:n.1799-14T>C
XM_011541429.1:c.1799-14T>C XP_011539731.1:n.1799-14T>C
XM_011541430.1:c.926-14T>C XP_011539732.1:n.926-14T>C
XM_011541431.1:c.65-14T>C XP_011539733.1:n.65-14T>C
XR_946650.1:n.1866-14T>C
NM_001364727.1:c.1484-14T>C NP_001351656.1:n.1484-14T>C
XM_005244749.3:c.1799-14T>C XP_005244806.1:n.1799-14T>C
XM_011541429.2:c.1799-14T>C XP_011539731.1:n.1799-14T>C
XR_946650.2:n.1870-14T>C
NM_001305275.2:c.1799-14T>C NP_001292204.1:n.1799-14T>C
NM_198576.4:c.1799-14T>C MANE Select NP_940978.2:n.1799-14T>C
NM_001364727.2:c.1484-14T>C NP_001351656.1:n.1484-14T>C