Canonical Allele Identifier: CA2839291304
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047968dup , CM000663.2:g.1047968dup GRCh38
NC_000001.10:g.983348dup , CM000663.1:g.983348dup GRCh37
NC_000001.9:g.973211dup NCBI36
NG_016346.1:g.32846dup , LRG_198:g.32846dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3752-44dup MANE Select ENSP00000368678.2:n.3752-44dup
ENST00000651234.1:c.3437-44dup ENSP00000499046.1:n.3437-44dup
ENST00000652369.1:c.3437-44dup ENSP00000498543.1:n.3437-44dup
ENST00000379370.6:c.3752-44dup ENSP00000368678.2:n.3752-44dup
ENST00000620552.4:c.3338-44dup ENSP00000484607.1:n.3338-44dup
NM_001305275.1:c.3752-44dup NP_001292204.1:n.3752-44dup
NM_198576.3:c.3752-44dup NP_940978.2:n.3752-44dup
XM_005244749.2:c.3752-44dup XP_005244806.1:n.3752-44dup
XM_006710635.2:c.3752-44dup XP_006710698.1:n.3752-44dup
XM_011541429.1:c.3752-44dup XP_011539731.1:n.3752-44dup
XM_011541430.1:c.2879-44dup XP_011539732.1:n.2879-44dup
XM_011541431.1:c.2018-44dup XP_011539733.1:n.2018-44dup
XR_946650.1:n.3819-44dup
NM_001364727.1:c.3437-44dup NP_001351656.1:n.3437-44dup
XM_005244749.3:c.3752-44dup XP_005244806.1:n.3752-44dup
XM_011541429.2:c.3752-44dup XP_011539731.1:n.3752-44dup
XR_946650.2:n.3823-44dup
NM_001305275.2:c.3752-44dup NP_001292204.1:n.3752-44dup
NM_198576.4:c.3752-44dup MANE Select NP_940978.2:n.3752-44dup
NM_001364727.2:c.3437-44dup NP_001351656.1:n.3437-44dup