Canonical Allele Identifier: CA2682048235

Gene: NPY

Linked Data

• gnomAD v4: 7-24285206-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285206C>T , CM000669.2:g.24285206C>T	GRCh38
NC_000007.13:g.24324825C>T , CM000669.1:g.24324825C>T	GRCh37
NC_000007.12:g.24291350C>T	NCBI36
NG_016148.1:g.6019C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-35C>T MANE Select	ENSP00000242152.2:n.1-35C>T
ENST00000242152.6:c.1-35C>T	ENSP00000242152.2:n.1-35C>T
ENST00000405982.1:c.-35C>T	ENSP00000385282.1:n.-35C>T
ENST00000407573.5:c.1-35C>T	ENSP00000384364.1:n.1-35C>T
NM_000905.3:c.1-35C>T	NP_000896.1:n.1-35C>T
XM_017012910.1:c.42-29507G>A	XP_016868399.1:n.42-29507G>A
XM_017012911.1:c.42-29507G>A	XP_016868400.1:n.42-29507G>A
XR_001745121.1:n.473+34151G>A
XR_001745122.1:n.345-88177G>A
XR_001745123.1:n.473+34151G>A
XR_001745124.1:n.473+34151G>A
XR_001745125.1:n.473+34151G>A
XR_001745126.1:n.473+34151G>A
XR_001745127.1:n.345-29507G>A
XR_001745129.1:n.473+34151G>A
XR_001745130.1:n.473+34151G>A
XR_001745131.1:n.473+34151G>A
XR_001745132.1:n.473+34151G>A
NM_000905.4:c.1-35C>T MANE Select	NP_000896.1:n.1-35C>T