Canonical Allele Identifier: CA454131918

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24325012G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285393G>T , CM000669.2:g.24285393G>T	GRCh38
NC_000007.13:g.24325012G>T , CM000669.1:g.24325012G>T	GRCh37
NC_000007.12:g.24291537G>T	NCBI36
NG_016148.1:g.6206G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.153G>T MANE Select	ENSP00000242152.2:p.Ala51=
ENST00000242152.6:c.153G>T	ENSP00000242152.2:p.Ala51=
ENST00000405982.1:c.153G>T	ENSP00000385282.1:p.Ala51=
ENST00000407573.5:c.153G>T	ENSP00000384364.1:p.Ala51=
NM_000905.3:c.153G>T	NP_000896.1:p.Ala51=
XM_017012910.1:c.42-29694C>A	XP_016868399.1:n.42-29694C>A
XM_017012911.1:c.42-29694C>A	XP_016868400.1:n.42-29694C>A
XR_001745121.1:n.473+33964C>A
XR_001745122.1:n.345-88364C>A
XR_001745123.1:n.473+33964C>A
XR_001745124.1:n.473+33964C>A
XR_001745125.1:n.473+33964C>A
XR_001745126.1:n.473+33964C>A
XR_001745127.1:n.345-29694C>A
XR_001745129.1:n.473+33964C>A
XR_001745130.1:n.473+33964C>A
XR_001745131.1:n.473+33964C>A
XR_001745132.1:n.473+33964C>A
NM_000905.4:c.153G>T MANE Select	NP_000896.1:p.Ala51=