Canonical Allele Identifier: CA2682047951

Gene: NPY

Linked Data

• gnomAD v4: 7-24285008-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285008A>T , CM000669.2:g.24285008A>T	GRCh38
NC_000007.13:g.24324627A>T , CM000669.1:g.24324627A>T	GRCh37
NC_000007.12:g.24291152A>T	NCBI36
NG_016148.1:g.5821A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-233A>T MANE Select	ENSP00000242152.2:n.1-233A>T
ENST00000242152.6:c.1-233A>T	ENSP00000242152.2:n.1-233A>T
ENST00000407573.5:c.-69A>T	ENSP00000384364.1:n.-69A>T
NM_000905.3:c.1-233A>T	NP_000896.1:n.1-233A>T
XM_017012910.1:c.42-29309T>A	XP_016868399.1:n.42-29309T>A
XM_017012911.1:c.42-29309T>A	XP_016868400.1:n.42-29309T>A
XR_001745121.1:n.473+34349T>A
XR_001745122.1:n.345-87979T>A
XR_001745123.1:n.473+34349T>A
XR_001745124.1:n.473+34349T>A
XR_001745125.1:n.473+34349T>A
XR_001745126.1:n.473+34349T>A
XR_001745127.1:n.345-29309T>A
XR_001745129.1:n.473+34349T>A
XR_001745130.1:n.473+34349T>A
XR_001745131.1:n.473+34349T>A
XR_001745132.1:n.473+34349T>A
NM_000905.4:c.1-233A>T MANE Select	NP_000896.1:n.1-233A>T