Canonical Allele Identifier: CA2682048950

Gene: NPY

Linked Data

• gnomAD v4: 7-24291859-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291859A>T , CM000669.2:g.24291859A>T	GRCh38
NC_000007.13:g.24331478A>T , CM000669.1:g.24331478A>T	GRCh37
NC_000007.12:g.24298003A>T	NCBI36
NG_016148.1:g.12672A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*172A>T MANE Select	ENSP00000242152.2:n.*172A>T
ENST00000242152.6:c.*172A>T	ENSP00000242152.2:n.*172A>T
NM_000905.3:c.*172A>T	NP_000896.1:n.*172A>T
XM_017012910.1:c.41+27498T>A	XP_016868399.1:n.41+27498T>A
XM_017012911.1:c.41+27498T>A	XP_016868400.1:n.41+27498T>A
XR_001745121.1:n.473+27498T>A
XR_001745122.1:n.345-94830T>A
XR_001745123.1:n.473+27498T>A
XR_001745124.1:n.473+27498T>A
XR_001745125.1:n.473+27498T>A
XR_001745126.1:n.473+27498T>A
XR_001745127.1:n.345-36160T>A
XR_001745129.1:n.473+27498T>A
XR_001745130.1:n.473+27498T>A
XR_001745131.1:n.473+27498T>A
XR_001745132.1:n.473+27498T>A
NM_000905.4:c.*172A>T MANE Select	NP_000896.1:n.*172A>T