Canonical Allele Identifier: CA1148804264
Gene: AGRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1022230A= , CM000663.2:g.1022230A= GRCh38
NC_000001.10:g.957610A= , CM000663.1:g.957610A= GRCh37
NC_000001.9:g.947473A= NCBI36
NG_016346.1:g.7108A= , LRG_198:g.7108A=

Transcript Alleles

HGVS Amino-acid change
ENST00000379370.7:c.231A= MANE Select ENSP00000368678.2:p.Lys77=
ENST00000379370.6:c.231A= ENSP00000368678.2:p.Lys77=
ENST00000620552.4:c.-184A= ENSP00000484607.1:n.-184A=
NM_001305275.1:c.231A= NP_001292204.1:p.Lys77=
NM_198576.3:c.231A= NP_940978.2:p.Lys77=
XM_005244749.2:c.231A= XP_005244806.1:p.Lys77=
XM_006710635.2:c.231A= XP_006710698.1:p.Lys77=
XM_011541429.1:c.231A= XP_011539731.1:p.Lys77=
XM_011541430.1:c.231A= XP_011539732.1:p.Lys77=
XR_946650.1:n.298A=
XM_005244749.3:c.231A= XP_005244806.1:p.Lys77=
XM_011541429.2:c.231A= XP_011539731.1:p.Lys77=
XR_946650.2:n.302A=
NM_001305275.2:c.231A= NP_001292204.1:p.Lys77=
NM_198576.4:c.231A= MANE Select NP_940978.2:p.Lys77=