Canonical Allele Identifier: CA2774746217

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290441C>A , CM000669.2:g.24290441C>A	GRCh38
NC_000007.13:g.24330060C>A , CM000669.1:g.24330060C>A	GRCh37
NC_000007.12:g.24296585C>A	NCBI36
NG_016148.1:g.11254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.269+862C>A MANE Select	ENSP00000242152.2:n.269+862C>A
ENST00000242152.6:c.269+862C>A	ENSP00000242152.2:n.269+862C>A
ENST00000405982.1:c.269+862C>A	ENSP00000385282.1:n.269+862C>A
ENST00000407573.5:c.269+862C>A	ENSP00000384364.1:n.269+862C>A
NM_000905.3:c.269+862C>A	NP_000896.1:n.269+862C>A
XM_017012910.1:c.41+28916G>T	XP_016868399.1:n.41+28916G>T
XM_017012911.1:c.41+28916G>T	XP_016868400.1:n.41+28916G>T
XR_001745121.1:n.473+28916G>T
XR_001745122.1:n.345-93412G>T
XR_001745123.1:n.473+28916G>T
XR_001745124.1:n.473+28916G>T
XR_001745125.1:n.473+28916G>T
XR_001745126.1:n.473+28916G>T
XR_001745127.1:n.345-34742G>T
XR_001745129.1:n.473+28916G>T
XR_001745130.1:n.473+28916G>T
XR_001745131.1:n.473+28916G>T
XR_001745132.1:n.473+28916G>T
NM_000905.4:c.269+862C>A MANE Select	NP_000896.1:n.269+862C>A