Canonical Allele Identifier: CA1694877496

Gene: NPY

Linked Data

• dbSNP Id: rs1787630851
• gnomAD v3: 7-24291857-T-G
• gnomAD v4: 7-24291857-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291857T>G , CM000669.2:g.24291857T>G	GRCh38
NC_000007.13:g.24331476T>G , CM000669.1:g.24331476T>G	GRCh37
NC_000007.12:g.24298001T>G	NCBI36
NG_016148.1:g.12670T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*170T>G MANE Select	ENSP00000242152.2:n.*170T>G
ENST00000242152.6:c.*170T>G	ENSP00000242152.2:n.*170T>G
NM_000905.3:c.*170T>G	NP_000896.1:n.*170T>G
XM_017012910.1:c.41+27500A>C	XP_016868399.1:n.41+27500A>C
XM_017012911.1:c.41+27500A>C	XP_016868400.1:n.41+27500A>C
XR_001745121.1:n.473+27500A>C
XR_001745122.1:n.345-94828A>C
XR_001745123.1:n.473+27500A>C
XR_001745124.1:n.473+27500A>C
XR_001745125.1:n.473+27500A>C
XR_001745126.1:n.473+27500A>C
XR_001745127.1:n.345-36158A>C
XR_001745129.1:n.473+27500A>C
XR_001745130.1:n.473+27500A>C
XR_001745131.1:n.473+27500A>C
XR_001745132.1:n.473+27500A>C
NM_000905.4:c.*170T>G MANE Select	NP_000896.1:n.*170T>G