Canonical Allele Identifier: CA1148802205
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1047867G= , CM000663.2:g.1047867G= GRCh38
NC_000001.10:g.983247G= , CM000663.1:g.983247G= GRCh37
NC_000001.9:g.973110G= NCBI36
NG_016346.1:g.32745G= , LRG_198:g.32745G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379370.7:c.3723G= MANE Select ENSP00000368678.2:p.Leu1241=
ENST00000651234.1:c.3408G= ENSP00000499046.1:p.Leu1136=
ENST00000652369.1:c.3408G= ENSP00000498543.1:p.Leu1136=
ENST00000379370.6:c.3723G= ENSP00000368678.2:p.Leu1241=
ENST00000620552.4:c.3309G= ENSP00000484607.1:p.Leu1103=
NM_001305275.1:c.3723G= NP_001292204.1:p.Leu1241=
NM_198576.3:c.3723G= NP_940978.2:p.Leu1241=
XM_005244749.2:c.3723G= XP_005244806.1:p.Leu1241=
XM_006710635.2:c.3723G= XP_006710698.1:p.Leu1241=
XM_011541429.1:c.3723G= XP_011539731.1:p.Leu1241=
XM_011541430.1:c.2850G= XP_011539732.1:p.Leu950=
XM_011541431.1:c.1989G= XP_011539733.1:p.Leu663=
XR_946650.1:n.3790G=
NM_001364727.1:c.3408G= NP_001351656.1:p.Leu1136=
XM_005244749.3:c.3723G= XP_005244806.1:p.Leu1241=
XM_011541429.2:c.3723G= XP_011539731.1:p.Leu1241=
XR_946650.2:n.3794G=
NM_001305275.2:c.3723G= NP_001292204.1:p.Leu1241=
NM_198576.4:c.3723G= MANE Select NP_940978.2:p.Leu1241=
NM_001364727.2:c.3408G= NP_001351656.1:p.Leu1136=