Canonical Allele Identifier: CA2682048908

Gene: NPY

Linked Data

• gnomAD v4: 7-24291823-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291823G>T , CM000669.2:g.24291823G>T	GRCh38
NC_000007.13:g.24331442G>T , CM000669.1:g.24331442G>T	GRCh37
NC_000007.12:g.24297967G>T	NCBI36
NG_016148.1:g.12636G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*136G>T MANE Select	ENSP00000242152.2:n.*136G>T
ENST00000242152.6:c.*136G>T	ENSP00000242152.2:n.*136G>T
ENST00000405982.1:c.*136G>T	ENSP00000385282.1:n.*136G>T
NM_000905.3:c.*136G>T	NP_000896.1:n.*136G>T
XM_017012910.1:c.41+27534C>A	XP_016868399.1:n.41+27534C>A
XM_017012911.1:c.41+27534C>A	XP_016868400.1:n.41+27534C>A
XR_001745121.1:n.473+27534C>A
XR_001745122.1:n.345-94794C>A
XR_001745123.1:n.473+27534C>A
XR_001745124.1:n.473+27534C>A
XR_001745125.1:n.473+27534C>A
XR_001745126.1:n.473+27534C>A
XR_001745127.1:n.345-36124C>A
XR_001745129.1:n.473+27534C>A
XR_001745130.1:n.473+27534C>A
XR_001745131.1:n.473+27534C>A
XR_001745132.1:n.473+27534C>A
NM_000905.4:c.*136G>T MANE Select	NP_000896.1:n.*136G>T