Canonical Allele Identifier: CA2682048191

Gene: NPY

Linked Data

• gnomAD v4: 7-24285158-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285158A>G , CM000669.2:g.24285158A>G	GRCh38
NC_000007.13:g.24324777A>G , CM000669.1:g.24324777A>G	GRCh37
NC_000007.12:g.24291302A>G	NCBI36
NG_016148.1:g.5971A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-83A>G MANE Select	ENSP00000242152.2:n.1-83A>G
ENST00000242152.6:c.1-83A>G	ENSP00000242152.2:n.1-83A>G
ENST00000405982.1:c.-83A>G	ENSP00000385282.1:n.-83A>G
ENST00000407573.5:c.1-83A>G	ENSP00000384364.1:n.1-83A>G
NM_000905.3:c.1-83A>G	NP_000896.1:n.1-83A>G
XM_017012910.1:c.42-29459T>C	XP_016868399.1:n.42-29459T>C
XM_017012911.1:c.42-29459T>C	XP_016868400.1:n.42-29459T>C
XR_001745121.1:n.473+34199T>C
XR_001745122.1:n.345-88129T>C
XR_001745123.1:n.473+34199T>C
XR_001745124.1:n.473+34199T>C
XR_001745125.1:n.473+34199T>C
XR_001745126.1:n.473+34199T>C
XR_001745127.1:n.345-29459T>C
XR_001745129.1:n.473+34199T>C
XR_001745130.1:n.473+34199T>C
XR_001745131.1:n.473+34199T>C
XR_001745132.1:n.473+34199T>C
NM_000905.4:c.1-83A>G MANE Select	NP_000896.1:n.1-83A>G