Canonical Allele Identifier: CA2841131147

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285208del , CM000669.2:g.24285208del	GRCh38
NC_000007.13:g.24324827del , CM000669.1:g.24324827del	GRCh37
NC_000007.12:g.24291352del	NCBI36
NG_016148.1:g.6021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-33del MANE Select	ENSP00000242152.2:n.1-33del
ENST00000242152.6:c.1-33del	ENSP00000242152.2:n.1-33del
ENST00000405982.1:c.-33del	ENSP00000385282.1:n.-33del
ENST00000407573.5:c.1-33del	ENSP00000384364.1:n.1-33del
NM_000905.3:c.1-33del	NP_000896.1:n.1-33del
XM_017012910.1:c.42-29506del	XP_016868399.1:n.42-29506del
XM_017012911.1:c.42-29506del	XP_016868400.1:n.42-29506del
XR_001745121.1:n.473+34152del
XR_001745122.1:n.345-88176del
XR_001745123.1:n.473+34152del
XR_001745124.1:n.473+34152del
XR_001745125.1:n.473+34152del
XR_001745126.1:n.473+34152del
XR_001745127.1:n.345-29506del
XR_001745129.1:n.473+34152del
XR_001745130.1:n.473+34152del
XR_001745131.1:n.473+34152del
XR_001745132.1:n.473+34152del
NM_000905.4:c.1-33del MANE Select	NP_000896.1:n.1-33del