Canonical Allele Identifier: CA2682048910
Gene: NPY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24291829_24291830dup , CM000669.2:g.24291829_24291830dup GRCh38
NC_000007.13:g.24331448_24331449dup , CM000669.1:g.24331448_24331449dup GRCh37
NC_000007.12:g.24297973_24297974dup NCBI36
NG_016148.1:g.12642_12643dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.7:c.*142_*143dup MANE Select ENSP00000242152.2:n.*142_*143dup
ENST00000242152.6:c.*142_*143dup ENSP00000242152.2:n.*142_*143dup
NM_000905.3:c.*142_*143dup NP_000896.1:n.*142_*143dup
XM_017012910.1:c.41+27532_41+27533dup XP_016868399.1:n.41+27532_41+27533dup
XM_017012911.1:c.41+27532_41+27533dup XP_016868400.1:n.41+27532_41+27533dup
XR_001745121.1:n.473+27532_473+27533dup
XR_001745122.1:n.345-94796_345-94795dup
XR_001745123.1:n.473+27532_473+27533dup
XR_001745124.1:n.473+27532_473+27533dup
XR_001745125.1:n.473+27532_473+27533dup
XR_001745126.1:n.473+27532_473+27533dup
XR_001745127.1:n.345-36126_345-36125dup
XR_001745129.1:n.473+27532_473+27533dup
XR_001745130.1:n.473+27532_473+27533dup
XR_001745131.1:n.473+27532_473+27533dup
XR_001745132.1:n.473+27532_473+27533dup
NM_000905.4:c.*142_*143dup MANE Select NP_000896.1:n.*142_*143dup