Canonical Allele Identifier: CA508437
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs770574780
gnomAD v4: 1-1044120-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1044120T>G , CM000663.2:g.1044120T>G GRCh38
NC_000001.10:g.979500T>G , CM000663.1:g.979500T>G GRCh37
NC_000001.9:g.969363T>G NCBI36
NG_016346.1:g.28998T>G , LRG_198:g.28998T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.2011T>G MANE Select ENSP00000368678.2:p.Ser671Ala
ENST00000651234.1:c.1696T>G ENSP00000499046.1:p.Ser566Ala
ENST00000652369.1:c.1696T>G ENSP00000498543.1:p.Ser566Ala
ENST00000379370.6:c.2011T>G ENSP00000368678.2:p.Ser671Ala
ENST00000620552.4:c.1597T>G ENSP00000484607.1:p.Ser533Ala
NM_001305275.1:c.2011T>G NP_001292204.1:p.Ser671Ala
NM_198576.3:c.2011T>G NP_940978.2:p.Ser671Ala
XM_005244749.2:c.2011T>G XP_005244806.1:p.Ser671Ala
XM_006710635.2:c.2011T>G XP_006710698.1:p.Ser671Ala
XM_011541429.1:c.2011T>G XP_011539731.1:p.Ser671Ala
XM_011541430.1:c.1138T>G XP_011539732.1:p.Ser380Ala
XM_011541431.1:c.277T>G XP_011539733.1:p.Ser93Ala
XR_946650.1:n.2078T>G
NM_001364727.1:c.1696T>G NP_001351656.1:p.Ser566Ala
XM_005244749.3:c.2011T>G XP_005244806.1:p.Ser671Ala
XM_011541429.2:c.2011T>G XP_011539731.1:p.Ser671Ala
XR_946650.2:n.2082T>G
NM_001305275.2:c.2011T>G NP_001292204.1:p.Ser671Ala
NM_198576.4:c.2011T>G MANE Select NP_940978.2:p.Ser671Ala
NM_001364727.2:c.1696T>G NP_001351656.1:p.Ser566Ala