Canonical Allele Identifier: CA2774746239

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291690G>A , CM000669.2:g.24291690G>A	GRCh38
NC_000007.13:g.24331309G>A , CM000669.1:g.24331309G>A	GRCh37
NC_000007.12:g.24297834G>A	NCBI36
NG_016148.1:g.12503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*3G>A MANE Select	ENSP00000242152.2:n.*3G>A
ENST00000242152.6:c.*3G>A	ENSP00000242152.2:n.*3G>A
ENST00000405982.1:c.*3G>A	ENSP00000385282.1:n.*3G>A
ENST00000407573.5:c.*3G>A	ENSP00000384364.1:n.*3G>A
NM_000905.3:c.*3G>A	NP_000896.1:n.*3G>A
XM_017012910.1:c.41+27667C>T	XP_016868399.1:n.41+27667C>T
XM_017012911.1:c.41+27667C>T	XP_016868400.1:n.41+27667C>T
XR_001745121.1:n.473+27667C>T
XR_001745122.1:n.345-94661C>T
XR_001745123.1:n.473+27667C>T
XR_001745124.1:n.473+27667C>T
XR_001745125.1:n.473+27667C>T
XR_001745126.1:n.473+27667C>T
XR_001745127.1:n.345-35991C>T
XR_001745129.1:n.473+27667C>T
XR_001745130.1:n.473+27667C>T
XR_001745131.1:n.473+27667C>T
XR_001745132.1:n.473+27667C>T
NM_000905.4:c.*3G>A MANE Select	NP_000896.1:n.*3G>A