Canonical Allele Identifier: CA495970763
Gene: AGRP HGNC NCBI
ATP6V0D1-DT HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.67516931T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67483028T>G , CM000678.2:g.67483028T>G GRCh38
NC_000016.9:g.67516931T>G , CM000678.1:g.67516931T>G GRCh37
NC_000016.8:g.66074432T>G NCBI36
NG_011482.1:g.3159A>C
NG_011501.1:g.5786A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000290953.3:c.213A>C (AGRP) MANE Select ENSP00000290953.3:p.Ala71=
ENST00000290953.2:c.213A>C (AGRP) ENSP00000290953.2:p.Ala71=
NM_001138.1:c.213A>C (AGRP) NP_001129.1:p.Ala71=
XM_011522927.1:c.213A>C (AGRP) XP_011521229.1:p.Ala71=
XR_243465.2:n.199-1082T>G (ATP6V0D1-DT)
XR_933690.1:n.200-1082T>G (ATP6V0D1-DT)
XR_933691.1:n.199-1082T>G (ATP6V0D1-DT)
XR_933692.1:n.201-1082T>G (ATP6V0D1-DT)
XR_001752246.1:n.194-1082T>G (ATP6V0D1-DT)
XR_001752247.1:n.194-1082T>G (ATP6V0D1-DT)
XR_001752248.1:n.196-1082T>G (ATP6V0D1-DT)
XR_001752249.1:n.194-1082T>G (ATP6V0D1-DT)
XR_001752250.1:n.194-1082T>G (ATP6V0D1-DT)
XR_933690.2:n.196-1082T>G (ATP6V0D1-DT)
XR_933691.2:n.202-1082T>G (ATP6V0D1-DT)
XR_933692.2:n.197-1082T>G (ATP6V0D1-DT)
NM_001138.2:c.213A>C (AGRP) MANE Select NP_001129.1:p.Ala71=