Canonical Allele Identifier: CA2529730880

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290788_24290790del , CM000669.2:g.24290788_24290790del	GRCh38
NC_000007.13:g.24330407_24330409del , CM000669.1:g.24330407_24330409del	GRCh37
NC_000007.12:g.24296932_24296934del	NCBI36
NG_016148.1:g.11601_11603del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-875_270-873del MANE Select	ENSP00000242152.2:n.270-875_270-873del
ENST00000242152.6:c.270-875_270-873del	ENSP00000242152.2:n.270-875_270-873del
ENST00000405982.1:c.270-875_270-873del	ENSP00000385282.1:n.270-875_270-873del
ENST00000407573.5:c.270-875_270-873del	ENSP00000384364.1:n.270-875_270-873del
NM_000905.3:c.270-875_270-873del	NP_000896.1:n.270-875_270-873del
XM_017012910.1:c.41+28579_41+28581del	XP_016868399.1:n.41+28579_41+28581del
XM_017012911.1:c.41+28579_41+28581del	XP_016868400.1:n.41+28579_41+28581del
XR_001745121.1:n.473+28579_473+28581del
XR_001745122.1:n.345-93749_345-93747del
XR_001745123.1:n.473+28579_473+28581del
XR_001745124.1:n.473+28579_473+28581del
XR_001745125.1:n.473+28579_473+28581del
XR_001745126.1:n.473+28579_473+28581del
XR_001745127.1:n.345-35079_345-35077del
XR_001745129.1:n.473+28579_473+28581del
XR_001745130.1:n.473+28579_473+28581del
XR_001745131.1:n.473+28579_473+28581del
XR_001745132.1:n.473+28579_473+28581del
NM_000905.4:c.270-875_270-873del MANE Select	NP_000896.1:n.270-875_270-873del