Canonical Allele Identifier: CA155829089

Gene: NPY

Linked Data

• dbSNP Id: rs371687880
• gnomAD v4: 7-24285298-G-A
• COSMIC: COSM1217754
• MyVariant Identifiers: chr7:g.24324917G>A (hg19) ; chr7:g.24285298G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285298G>A , CM000669.2:g.24285298G>A	GRCh38
NC_000007.13:g.24324917G>A , CM000669.1:g.24324917G>A	GRCh37
NC_000007.12:g.24291442G>A	NCBI36
NG_016148.1:g.6111G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.58G>A MANE Select	ENSP00000242152.2:p.Val20Met
ENST00000242152.6:c.58G>A	ENSP00000242152.2:p.Val20Met
ENST00000405982.1:c.58G>A	ENSP00000385282.1:p.Val20Met
ENST00000407573.5:c.58G>A	ENSP00000384364.1:p.Val20Met
NM_000905.3:c.58G>A	NP_000896.1:p.Val20Met
XM_017012910.1:c.42-29599C>T	XP_016868399.1:n.42-29599C>T
XM_017012911.1:c.42-29599C>T	XP_016868400.1:n.42-29599C>T
XR_001745121.1:n.473+34059C>T
XR_001745122.1:n.345-88269C>T
XR_001745123.1:n.473+34059C>T
XR_001745124.1:n.473+34059C>T
XR_001745125.1:n.473+34059C>T
XR_001745126.1:n.473+34059C>T
XR_001745127.1:n.345-29599C>T
XR_001745129.1:n.473+34059C>T
XR_001745130.1:n.473+34059C>T
XR_001745131.1:n.473+34059C>T
XR_001745132.1:n.473+34059C>T
NM_000905.4:c.58G>A MANE Select	NP_000896.1:p.Val20Met