Canonical Allele Identifier: CA1148747445
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1049927_1049942delinsGCCCCTGCCAGCCCAA , CM000663.2:g.1049927_1049942delinsGCCCCTGCCAGCCCAA GRCh38
NC_000001.10:g.985307_985322delinsGCCCCTGCCAGCCCAA , CM000663.1:g.985307_985322delinsGCCCCTGCCAGCCCAA GRCh37
NC_000001.9:g.975170_975185delinsGCCCCTGCCAGCCCAA NCBI36
NG_016346.1:g.34805_34820delinsGCCCCTGCCAGCCCAA , LRG_198:g.34805_34820delinsGCCCCTGCCAGCCCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4769_4784delinsGCCCCTGCCAGCCCAA MANE Select ENSP00000368678.2:p.Ser1590=
ENST00000651234.1:c.4454_4469delinsGCCCCTGCCAGCCCAA ENSP00000499046.1:p.Ser1485=
ENST00000652369.1:c.4454_4469delinsGCCCCTGCCAGCCCAA ENSP00000498543.1:p.Ser1485=
ENST00000379370.6:c.4769_4784delinsGCCCCTGCCAGCCCAA ENSP00000368678.2:p.Ser1590=
ENST00000620552.4:c.4355_4370delinsGCCCCTGCCAGCCCAA ENSP00000484607.1:p.Ser1452=
NM_001305275.1:c.4769_4784delinsGCCCCTGCCAGCCCAA NP_001292204.1:p.Ser1590=
NM_198576.3:c.4769_4784delinsGCCCCTGCCAGCCCAA NP_940978.2:p.Ser1590=
XM_005244749.2:c.4769_4784delinsGCCCCTGCCAGCCCAA XP_005244806.1:p.Ser1590=
XM_006710635.2:c.4769_4784delinsGCCCCTGCCAGCCCAA XP_006710698.1:p.Ser1590=
XM_011541429.1:c.4769_4784delinsGCCCCTGCCAGCCCAA XP_011539731.1:p.Ser1590=
XM_011541430.1:c.3896_3911delinsGCCCCTGCCAGCCCAA XP_011539732.1:p.Ser1299=
XM_011541431.1:c.3035_3050delinsGCCCCTGCCAGCCCAA XP_011539733.1:p.Ser1012=
XR_946650.1:n.4836_4851delinsGCCCCTGCCAGCCCAA
NM_001364727.1:c.4454_4469delinsGCCCCTGCCAGCCCAA NP_001351656.1:p.Ser1485=
XM_005244749.3:c.4769_4784delinsGCCCCTGCCAGCCCAA XP_005244806.1:p.Ser1590=
XM_011541429.2:c.4769_4784delinsGCCCCTGCCAGCCCAA XP_011539731.1:p.Ser1590=
XR_946650.2:n.4840_4855delinsGCCCCTGCCAGCCCAA
NM_001305275.2:c.4769_4784delinsGCCCCTGCCAGCCCAA NP_001292204.1:p.Ser1590=
NM_198576.4:c.4769_4784delinsGCCCCTGCCAGCCCAA MANE Select NP_940978.2:p.Ser1590=
NM_001364727.2:c.4454_4469delinsGCCCCTGCCAGCCCAA NP_001351656.1:p.Ser1485=