Canonical Allele Identifier: CA2580714112

Gene: NPY

Linked Data

• gnomAD v4: 7-24285189-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285189C>A , CM000669.2:g.24285189C>A	GRCh38
NC_000007.13:g.24324808C>A , CM000669.1:g.24324808C>A	GRCh37
NC_000007.12:g.24291333C>A	NCBI36
NG_016148.1:g.6002C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-52C>A MANE Select	ENSP00000242152.2:n.1-52C>A
ENST00000242152.6:c.1-52C>A	ENSP00000242152.2:n.1-52C>A
ENST00000405982.1:c.-52C>A	ENSP00000385282.1:n.-52C>A
ENST00000407573.5:c.1-52C>A	ENSP00000384364.1:n.1-52C>A
NM_000905.3:c.1-52C>A	NP_000896.1:n.1-52C>A
XM_017012910.1:c.42-29490G>T	XP_016868399.1:n.42-29490G>T
XM_017012911.1:c.42-29490G>T	XP_016868400.1:n.42-29490G>T
XR_001745121.1:n.473+34168G>T
XR_001745122.1:n.345-88160G>T
XR_001745123.1:n.473+34168G>T
XR_001745124.1:n.473+34168G>T
XR_001745125.1:n.473+34168G>T
XR_001745126.1:n.473+34168G>T
XR_001745127.1:n.345-29490G>T
XR_001745129.1:n.473+34168G>T
XR_001745130.1:n.473+34168G>T
XR_001745131.1:n.473+34168G>T
XR_001745132.1:n.473+34168G>T
NM_000905.4:c.1-52C>A MANE Select	NP_000896.1:n.1-52C>A