Canonical Allele Identifier: CA337853183
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs1418859536
gnomAD v2: 1-983607-C-T
gnomAD v3: 1-1048227-C-T
gnomAD v4: 1-1048227-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1048227C>T , CM000663.2:g.1048227C>T GRCh38
NC_000001.10:g.983607C>T , CM000663.1:g.983607C>T GRCh37
NC_000001.9:g.973470C>T NCBI36
NG_016346.1:g.33105C>T , LRG_198:g.33105C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3967C>T MANE Select ENSP00000368678.2:p.Pro1323Ser
ENST00000651234.1:c.3652C>T ENSP00000499046.1:p.Pro1218Ser
ENST00000652369.1:c.3652C>T ENSP00000498543.1:p.Pro1218Ser
ENST00000379370.6:c.3967C>T ENSP00000368678.2:p.Pro1323Ser
ENST00000620552.4:c.3553C>T ENSP00000484607.1:p.Pro1185Ser
NM_001305275.1:c.3967C>T NP_001292204.1:p.Pro1323Ser
NM_198576.3:c.3967C>T NP_940978.2:p.Pro1323Ser
XM_005244749.2:c.3967C>T XP_005244806.1:p.Pro1323Ser
XM_006710635.2:c.3967C>T XP_006710698.1:p.Pro1323Ser
XM_011541429.1:c.3967C>T XP_011539731.1:p.Pro1323Ser
XM_011541430.1:c.3094C>T XP_011539732.1:p.Pro1032Ser
XM_011541431.1:c.2233C>T XP_011539733.1:p.Pro745Ser
XR_946650.1:n.4034C>T
NM_001364727.1:c.3652C>T NP_001351656.1:p.Pro1218Ser
XM_005244749.3:c.3967C>T XP_005244806.1:p.Pro1323Ser
XM_011541429.2:c.3967C>T XP_011539731.1:p.Pro1323Ser
XR_946650.2:n.4038C>T
NM_001305275.2:c.3967C>T NP_001292204.1:p.Pro1323Ser
NM_198576.4:c.3967C>T MANE Select NP_940978.2:p.Pro1323Ser
NM_001364727.2:c.3652C>T NP_001351656.1:p.Pro1218Ser