Canonical Allele Identifier: CA2682048135
Gene: NPY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24285133_24285134del , CM000669.2:g.24285133_24285134del GRCh38
NC_000007.13:g.24324752_24324753del , CM000669.1:g.24324752_24324753del GRCh37
NC_000007.12:g.24291277_24291278del NCBI36
NG_016148.1:g.5946_5947del

Transcript Alleles

HGVS Amino-acid change
ENST00000242152.7:c.1-108_1-107del MANE Select ENSP00000242152.2:n.1-108_1-107del
ENST00000242152.6:c.1-108_1-107del ENSP00000242152.2:n.1-108_1-107del
ENST00000405982.1:c.-108_-107del ENSP00000385282.1:n.-108_-107del
ENST00000407573.5:c.-1+57_-1+58del ENSP00000384364.1:n.-1+57_-1+58del
NM_000905.3:c.1-108_1-107del NP_000896.1:n.1-108_1-107del
XM_017012910.1:c.42-29432_42-29431del XP_016868399.1:n.42-29432_42-29431del
XM_017012911.1:c.42-29432_42-29431del XP_016868400.1:n.42-29432_42-29431del
XR_001745121.1:n.473+34226_473+34227del
XR_001745122.1:n.345-88102_345-88101del
XR_001745123.1:n.473+34226_473+34227del
XR_001745124.1:n.473+34226_473+34227del
XR_001745125.1:n.473+34226_473+34227del
XR_001745126.1:n.473+34226_473+34227del
XR_001745127.1:n.345-29432_345-29431del
XR_001745129.1:n.473+34226_473+34227del
XR_001745130.1:n.473+34226_473+34227del
XR_001745131.1:n.473+34226_473+34227del
XR_001745132.1:n.473+34226_473+34227del
NM_000905.4:c.1-108_1-107del MANE Select NP_000896.1:n.1-108_1-107del