Canonical Allele Identifier: CA396268140
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67482688A>G , CM000678.2:g.67482688A>G GRCh38
NC_000016.9:g.67516591A>G , CM000678.1:g.67516591A>G GRCh37
NC_000016.8:g.66074092A>G NCBI36
NG_011482.1:g.3499T>C
NG_011501.1:g.6126T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.347T>C (AGRP) MANE Select ENSP00000290953.3:p.Phe116Ser
ENST00000290953.2:c.347T>C (AGRP) ENSP00000290953.2:p.Phe116Ser
NM_001138.1:c.347T>C (AGRP) NP_001129.1:p.Phe116Ser
XM_011522927.1:c.347T>C (AGRP) XP_011521229.1:p.Phe116Ser
XR_243465.2:n.198+1169A>G (ATP6V0D1-DT)
XR_933690.1:n.199+1169A>G (ATP6V0D1-DT)
XR_933691.1:n.198+1169A>G (ATP6V0D1-DT)
XR_933692.1:n.200+1169A>G (ATP6V0D1-DT)
XR_001752246.1:n.193+1169A>G (ATP6V0D1-DT)
XR_001752247.1:n.193+1169A>G (ATP6V0D1-DT)
XR_001752248.1:n.195+1169A>G (ATP6V0D1-DT)
XR_001752249.1:n.193+1169A>G (ATP6V0D1-DT)
XR_001752250.1:n.193+1169A>G (ATP6V0D1-DT)
XR_933690.2:n.195+1169A>G (ATP6V0D1-DT)
XR_933691.2:n.201+1169A>G (ATP6V0D1-DT)
XR_933692.2:n.196+1169A>G (ATP6V0D1-DT)
NM_001138.2:c.347T>C (AGRP) MANE Select NP_001129.1:p.Phe116Ser