Canonical Allele Identifier: CA16701032
Gene: AGRN HGNC NCBI

Linked Data

dbSNP Id: rs36102650

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1050250dup , CM000663.2:g.1050250dup GRCh38
NC_000001.10:g.985630dup , CM000663.1:g.985630dup GRCh37
NC_000001.9:g.975493dup NCBI36
NG_016346.1:g.35128dup , LRG_198:g.35128dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.4897dup MANE Select ENSP00000368678.2:p.Ser1633PhefsTer7
ENST00000651234.1:c.4582dup ENSP00000499046.1:p.Ser1528PhefsTer7
ENST00000652369.1:c.4582dup ENSP00000498543.1:p.Ser1528PhefsTer7
ENST00000379370.6:c.4897dup ENSP00000368678.2:p.Ser1633PhefsTer7
ENST00000620552.4:c.4483dup ENSP00000484607.1:p.Ser1495PhefsTer7
NM_001305275.1:c.4897dup NP_001292204.1:p.Ser1633PhefsTer7
NM_198576.3:c.4897dup NP_940978.2:p.Ser1633PhefsTer7
XM_005244749.2:c.4897dup XP_005244806.1:p.Ser1633PhefsTer7
XM_006710635.2:c.4897dup XP_006710698.1:p.Ser1633PhefsTer7
XM_011541429.1:c.4897dup XP_011539731.1:p.Ser1633PhefsTer7
XM_011541430.1:c.4024dup XP_011539732.1:p.Ser1342PhefsTer7
XM_011541431.1:c.3163dup XP_011539733.1:p.Ser1055PhefsTer7
XR_946650.1:n.4964dup
NM_001364727.1:c.4582dup NP_001351656.1:p.Ser1528PhefsTer7
XM_005244749.3:c.4897dup XP_005244806.1:p.Ser1633PhefsTer7
XM_011541429.2:c.4897dup XP_011539731.1:p.Ser1633PhefsTer7
XR_946650.2:n.4968dup
NM_001305275.2:c.4897dup NP_001292204.1:p.Ser1633PhefsTer7
NM_198576.4:c.4897dup MANE Select NP_940978.2:p.Ser1633PhefsTer7
NM_001364727.2:c.4582dup NP_001351656.1:p.Ser1528PhefsTer7