Canonical Allele Identifier: CA1694876929

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290759_24290768delinsAAATAATAAT , CM000669.2:g.24290759_24290768delinsAAATAATAAT	GRCh38
NC_000007.13:g.24330378_24330387delinsAAATAATAAT , CM000669.1:g.24330378_24330387delinsAAATAATAAT	GRCh37
NC_000007.12:g.24296903_24296912delinsAAATAATAAT	NCBI36
NG_016148.1:g.11572_11581delinsAAATAATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-904_270-895delinsAAATAATAAT MANE Select	ENSP00000242152.2:n.270-904_270-895delinsAAATAATAAT
ENST00000242152.6:c.270-904_270-895delinsAAATAATAAT	ENSP00000242152.2:n.270-904_270-895delinsAAATAATAAT
ENST00000405982.1:c.270-904_270-895delinsAAATAATAAT	ENSP00000385282.1:n.270-904_270-895delinsAAATAATAAT
ENST00000407573.5:c.270-904_270-895delinsAAATAATAAT	ENSP00000384364.1:n.270-904_270-895delinsAAATAATAAT
NM_000905.3:c.270-904_270-895delinsAAATAATAAT	NP_000896.1:n.270-904_270-895delinsAAATAATAAT
XM_017012910.1:c.41+28589_41+28598delinsATTATTATTT	XP_016868399.1:n.41+28589_41+28598delinsATTATTATTT
XM_017012911.1:c.41+28589_41+28598delinsATTATTATTT	XP_016868400.1:n.41+28589_41+28598delinsATTATTATTT
XR_001745121.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745122.1:n.345-93739_345-93730delinsATTATTATTT
XR_001745123.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745124.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745125.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745126.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745127.1:n.345-35069_345-35060delinsATTATTATTT
XR_001745129.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745130.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745131.1:n.473+28589_473+28598delinsATTATTATTT
XR_001745132.1:n.473+28589_473+28598delinsATTATTATTT
NM_000905.4:c.270-904_270-895delinsAAATAATAAT MANE Select	NP_000896.1:n.270-904_270-895delinsAAATAATAAT