Canonical Allele Identifier: CA2682047962

Gene: NPY

Linked Data

• gnomAD v4: 7-24285016-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285016C>A , CM000669.2:g.24285016C>A	GRCh38
NC_000007.13:g.24324635C>A , CM000669.1:g.24324635C>A	GRCh37
NC_000007.12:g.24291160C>A	NCBI36
NG_016148.1:g.5829C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-225C>A MANE Select	ENSP00000242152.2:n.1-225C>A
ENST00000242152.6:c.1-225C>A	ENSP00000242152.2:n.1-225C>A
ENST00000407573.5:c.-61C>A	ENSP00000384364.1:n.-61C>A
NM_000905.3:c.1-225C>A	NP_000896.1:n.1-225C>A
XM_017012910.1:c.42-29317G>T	XP_016868399.1:n.42-29317G>T
XM_017012911.1:c.42-29317G>T	XP_016868400.1:n.42-29317G>T
XR_001745121.1:n.473+34341G>T
XR_001745122.1:n.345-87987G>T
XR_001745123.1:n.473+34341G>T
XR_001745124.1:n.473+34341G>T
XR_001745125.1:n.473+34341G>T
XR_001745126.1:n.473+34341G>T
XR_001745127.1:n.345-29317G>T
XR_001745129.1:n.473+34341G>T
XR_001745130.1:n.473+34341G>T
XR_001745131.1:n.473+34341G>T
XR_001745132.1:n.473+34341G>T
NM_000905.4:c.1-225C>A MANE Select	NP_000896.1:n.1-225C>A