Canonical Allele Identifier: CA396268145
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67482689A>C , CM000678.2:g.67482689A>C GRCh38
NC_000016.9:g.67516592A>C , CM000678.1:g.67516592A>C GRCh37
NC_000016.8:g.66074093A>C NCBI36
NG_011482.1:g.3498T>G
NG_011501.1:g.6125T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.346T>G (AGRP) MANE Select ENSP00000290953.3:p.Phe116Val
ENST00000290953.2:c.346T>G (AGRP) ENSP00000290953.2:p.Phe116Val
NM_001138.1:c.346T>G (AGRP) NP_001129.1:p.Phe116Val
XM_011522927.1:c.346T>G (AGRP) XP_011521229.1:p.Phe116Val
XR_243465.2:n.198+1170A>C (ATP6V0D1-DT)
XR_933690.1:n.199+1170A>C (ATP6V0D1-DT)
XR_933691.1:n.198+1170A>C (ATP6V0D1-DT)
XR_933692.1:n.200+1170A>C (ATP6V0D1-DT)
XR_001752246.1:n.193+1170A>C (ATP6V0D1-DT)
XR_001752247.1:n.193+1170A>C (ATP6V0D1-DT)
XR_001752248.1:n.195+1170A>C (ATP6V0D1-DT)
XR_001752249.1:n.193+1170A>C (ATP6V0D1-DT)
XR_001752250.1:n.193+1170A>C (ATP6V0D1-DT)
XR_933690.2:n.195+1170A>C (ATP6V0D1-DT)
XR_933691.2:n.201+1170A>C (ATP6V0D1-DT)
XR_933692.2:n.196+1170A>C (ATP6V0D1-DT)
NM_001138.2:c.346T>G (AGRP) MANE Select NP_001129.1:p.Phe116Val