Canonical Allele Identifier: CA2682048048

Gene: NPY

Linked Data

• gnomAD v4: 7-24285065-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285065G>T , CM000669.2:g.24285065G>T	GRCh38
NC_000007.13:g.24324684G>T , CM000669.1:g.24324684G>T	GRCh37
NC_000007.12:g.24291209G>T	NCBI36
NG_016148.1:g.5878G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-176G>T MANE Select	ENSP00000242152.2:n.1-176G>T
ENST00000242152.6:c.1-176G>T	ENSP00000242152.2:n.1-176G>T
ENST00000407573.5:c.-12G>T	ENSP00000384364.1:n.-12G>T
NM_000905.3:c.1-176G>T	NP_000896.1:n.1-176G>T
XM_017012910.1:c.42-29366C>A	XP_016868399.1:n.42-29366C>A
XM_017012911.1:c.42-29366C>A	XP_016868400.1:n.42-29366C>A
XR_001745121.1:n.473+34292C>A
XR_001745122.1:n.345-88036C>A
XR_001745123.1:n.473+34292C>A
XR_001745124.1:n.473+34292C>A
XR_001745125.1:n.473+34292C>A
XR_001745126.1:n.473+34292C>A
XR_001745127.1:n.345-29366C>A
XR_001745129.1:n.473+34292C>A
XR_001745130.1:n.473+34292C>A
XR_001745131.1:n.473+34292C>A
XR_001745132.1:n.473+34292C>A
NM_000905.4:c.1-176G>T MANE Select	NP_000896.1:n.1-176G>T