Canonical Allele Identifier: CA2682047965

Gene: NPY

Linked Data

• gnomAD v4: 7-24285019-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285019A>C , CM000669.2:g.24285019A>C	GRCh38
NC_000007.13:g.24324638A>C , CM000669.1:g.24324638A>C	GRCh37
NC_000007.12:g.24291163A>C	NCBI36
NG_016148.1:g.5832A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-222A>C MANE Select	ENSP00000242152.2:n.1-222A>C
ENST00000242152.6:c.1-222A>C	ENSP00000242152.2:n.1-222A>C
ENST00000407573.5:c.-58A>C	ENSP00000384364.1:n.-58A>C
NM_000905.3:c.1-222A>C	NP_000896.1:n.1-222A>C
XM_017012910.1:c.42-29320T>G	XP_016868399.1:n.42-29320T>G
XM_017012911.1:c.42-29320T>G	XP_016868400.1:n.42-29320T>G
XR_001745121.1:n.473+34338T>G
XR_001745122.1:n.345-87990T>G
XR_001745123.1:n.473+34338T>G
XR_001745124.1:n.473+34338T>G
XR_001745125.1:n.473+34338T>G
XR_001745126.1:n.473+34338T>G
XR_001745127.1:n.345-29320T>G
XR_001745129.1:n.473+34338T>G
XR_001745130.1:n.473+34338T>G
XR_001745131.1:n.473+34338T>G
XR_001745132.1:n.473+34338T>G
NM_000905.4:c.1-222A>C MANE Select	NP_000896.1:n.1-222A>C