Canonical Allele Identifier: CA367052258

Gene: NPY

Linked Data

• dbSNP Id: rs753866284
• gnomAD v3: 7-24291671-A-T
• gnomAD v4: 7-24291671-A-T
• MyVariant Identifiers: chr7:g.24331290A>T (hg19) ; chr7:g.24291671A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291671A>T , CM000669.2:g.24291671A>T	GRCh38
NC_000007.13:g.24331290A>T , CM000669.1:g.24331290A>T	GRCh37
NC_000007.12:g.24297815A>T	NCBI36
NG_016148.1:g.12484A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.278A>T MANE Select	ENSP00000242152.2:p.Asp93Val
ENST00000242152.6:c.278A>T	ENSP00000242152.2:p.Asp93Val
ENST00000405982.1:c.278A>T	ENSP00000385282.1:p.Asp93Val
ENST00000407573.5:c.278A>T	ENSP00000384364.1:p.Asp93Val
NM_000905.3:c.278A>T	NP_000896.1:p.Asp93Val
XM_017012910.1:c.41+27686T>A	XP_016868399.1:n.41+27686T>A
XM_017012911.1:c.41+27686T>A	XP_016868400.1:n.41+27686T>A
XR_001745121.1:n.473+27686T>A
XR_001745122.1:n.345-94642T>A
XR_001745123.1:n.473+27686T>A
XR_001745124.1:n.473+27686T>A
XR_001745125.1:n.473+27686T>A
XR_001745126.1:n.473+27686T>A
XR_001745127.1:n.345-35972T>A
XR_001745129.1:n.473+27686T>A
XR_001745130.1:n.473+27686T>A
XR_001745131.1:n.473+27686T>A
XR_001745132.1:n.473+27686T>A
NM_000905.4:c.278A>T MANE Select	NP_000896.1:p.Asp93Val