Canonical Allele Identifier: CA2229344228
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67482658A= , CM000678.2:g.67482658A= GRCh38
NC_000016.9:g.67516561A= , CM000678.1:g.67516561A= GRCh37
NC_000016.8:g.66074062A= NCBI36
NG_011482.1:g.3529T=
NG_011501.1:g.6156T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.377T= (AGRP) MANE Select ENSP00000290953.3:p.Met126=
ENST00000290953.2:c.377T= (AGRP) ENSP00000290953.2:p.Met126=
NM_001138.1:c.377T= (AGRP) NP_001129.1:p.Met126=
XM_011522927.1:c.377T= (AGRP) XP_011521229.1:p.Met126=
XR_243465.2:n.198+1139A= (ATP6V0D1-DT)
XR_933690.1:n.199+1139A= (ATP6V0D1-DT)
XR_933691.1:n.198+1139A= (ATP6V0D1-DT)
XR_933692.1:n.200+1139A= (ATP6V0D1-DT)
XR_001752246.1:n.193+1139A= (ATP6V0D1-DT)
XR_001752247.1:n.193+1139A= (ATP6V0D1-DT)
XR_001752248.1:n.195+1139A= (ATP6V0D1-DT)
XR_001752249.1:n.193+1139A= (ATP6V0D1-DT)
XR_001752250.1:n.193+1139A= (ATP6V0D1-DT)
XR_933690.2:n.195+1139A= (ATP6V0D1-DT)
XR_933691.2:n.201+1139A= (ATP6V0D1-DT)
XR_933692.2:n.196+1139A= (ATP6V0D1-DT)
NM_001138.2:c.377T= (AGRP) MANE Select NP_001129.1:p.Met126=