Canonical Allele Identifier: CA367052258
Gene: NPY HGNC NCBI

Linked Data

dbSNP Id: rs753866284
gnomAD v3: 7-24291671-A-T
gnomAD v4: 7-24291671-A-T

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