Canonical Allele Identifier: CA454131924

Gene: NPY

Linked Data

• gnomAD v4: 7-24285397-C-A
• MyVariant Identifiers: chr7:g.24325016C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285397C>A , CM000669.2:g.24285397C>A	GRCh38
NC_000007.13:g.24325016C>A , CM000669.1:g.24325016C>A	GRCh37
NC_000007.12:g.24291541C>A	NCBI36
NG_016148.1:g.6210C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.157C>A MANE Select	ENSP00000242152.2:p.Arg53=
ENST00000242152.6:c.157C>A	ENSP00000242152.2:p.Arg53=
ENST00000405982.1:c.157C>A	ENSP00000385282.1:p.Arg53=
ENST00000407573.5:c.157C>A	ENSP00000384364.1:p.Arg53=
NM_000905.3:c.157C>A	NP_000896.1:p.Arg53=
XM_017012910.1:c.42-29698G>T	XP_016868399.1:n.42-29698G>T
XM_017012911.1:c.42-29698G>T	XP_016868400.1:n.42-29698G>T
XR_001745121.1:n.473+33960G>T
XR_001745122.1:n.345-88368G>T
XR_001745123.1:n.473+33960G>T
XR_001745124.1:n.473+33960G>T
XR_001745125.1:n.473+33960G>T
XR_001745126.1:n.473+33960G>T
XR_001745127.1:n.345-29698G>T
XR_001745129.1:n.473+33960G>T
XR_001745130.1:n.473+33960G>T
XR_001745131.1:n.473+33960G>T
XR_001745132.1:n.473+33960G>T
NM_000905.4:c.157C>A MANE Select	NP_000896.1:p.Arg53=