Canonical Allele Identifier: CA1148804267
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1022231G= , CM000663.2:g.1022231G= GRCh38
NC_000001.10:g.957611G= , CM000663.1:g.957611G= GRCh37
NC_000001.9:g.947474G= NCBI36
NG_016346.1:g.7109G= , LRG_198:g.7109G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379370.7:c.232G= MANE Select ENSP00000368678.2:p.Asp78=
ENST00000379370.6:c.232G= ENSP00000368678.2:p.Asp78=
ENST00000620552.4:c.-183G= ENSP00000484607.1:n.-183G=
NM_001305275.1:c.232G= NP_001292204.1:p.Asp78=
NM_198576.3:c.232G= NP_940978.2:p.Asp78=
XM_005244749.2:c.232G= XP_005244806.1:p.Asp78=
XM_006710635.2:c.232G= XP_006710698.1:p.Asp78=
XM_011541429.1:c.232G= XP_011539731.1:p.Asp78=
XM_011541430.1:c.232G= XP_011539732.1:p.Asp78=
XR_946650.1:n.299G=
XM_005244749.3:c.232G= XP_005244806.1:p.Asp78=
XM_011541429.2:c.232G= XP_011539731.1:p.Asp78=
XR_946650.2:n.303G=
NM_001305275.2:c.232G= NP_001292204.1:p.Asp78=
NM_198576.4:c.232G= MANE Select NP_940978.2:p.Asp78=