Canonical Allele Identifier: CA2682048179
Gene: NPY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24285155_24285181del , CM000669.2:g.24285155_24285181del GRCh38
NC_000007.13:g.24324774_24324800del , CM000669.1:g.24324774_24324800del GRCh37
NC_000007.12:g.24291299_24291325del NCBI36
NG_016148.1:g.5968_5994del

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.1-86_1-60del MANE Select ENSP00000242152.2:n.1-86_1-60del
ENST00000242152.6:c.1-86_1-60del ENSP00000242152.2:n.1-86_1-60del
ENST00000405982.1:c.-86_-60del ENSP00000385282.1:n.-86_-60del
ENST00000407573.5:c.-1+79_1-60del ENSP00000384364.1:n.-1+79_1-60del
NM_000905.3:c.1-86_1-60del NP_000896.1:n.1-86_1-60del
XM_017012910.1:c.42-29477_42-29451del XP_016868399.1:n.42-29477_42-29451del
XM_017012911.1:c.42-29477_42-29451del XP_016868400.1:n.42-29477_42-29451del
XR_001745121.1:n.473+34181_473+34207del
XR_001745122.1:n.345-88147_345-88121del
XR_001745123.1:n.473+34181_473+34207del
XR_001745124.1:n.473+34181_473+34207del
XR_001745125.1:n.473+34181_473+34207del
XR_001745126.1:n.473+34181_473+34207del
XR_001745127.1:n.345-29477_345-29451del
XR_001745129.1:n.473+34181_473+34207del
XR_001745130.1:n.473+34181_473+34207del
XR_001745131.1:n.473+34181_473+34207del
XR_001745132.1:n.473+34181_473+34207del
NM_000905.4:c.1-86_1-60del MANE Select NP_000896.1:n.1-86_1-60del