Canonical Allele Identifier: CA4190810

Gene: NPY

Linked Data

• dbSNP Id: rs78838996
• ExAC: 7:24331286 G / T
• gnomAD v2: 7-24331286-G-T
• MyVariant Identifiers: chr7:g.24331286G>T (hg19) ; chr7:g.24291667G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291667G>T , CM000669.2:g.24291667G>T	GRCh38
NC_000007.13:g.24331286G>T , CM000669.1:g.24331286G>T	GRCh37
NC_000007.12:g.24297811G>T	NCBI36
NG_016148.1:g.12480G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.274G>T MANE Select	ENSP00000242152.2:p.Glu92Ter
ENST00000242152.6:c.274G>T	ENSP00000242152.2:p.Glu92Ter
ENST00000405982.1:c.274G>T	ENSP00000385282.1:p.Glu92Ter
ENST00000407573.5:c.274G>T	ENSP00000384364.1:p.Glu92Ter
NM_000905.3:c.274G>T	NP_000896.1:p.Glu92Ter
XM_017012910.1:c.41+27690C>A	XP_016868399.1:n.41+27690C>A
XM_017012911.1:c.41+27690C>A	XP_016868400.1:n.41+27690C>A
XR_001745121.1:n.473+27690C>A
XR_001745122.1:n.345-94638C>A
XR_001745123.1:n.473+27690C>A
XR_001745124.1:n.473+27690C>A
XR_001745125.1:n.473+27690C>A
XR_001745126.1:n.473+27690C>A
XR_001745127.1:n.345-35968C>A
XR_001745129.1:n.473+27690C>A
XR_001745130.1:n.473+27690C>A
XR_001745131.1:n.473+27690C>A
XR_001745132.1:n.473+27690C>A
NM_000905.4:c.274G>T MANE Select	NP_000896.1:p.Glu92Ter