Canonical Allele Identifier: CA367051970

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24325016C>G (hg19) ; chr7:g.24285397C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.157C>G MANE Select	ENSP00000242152.2:p.Arg53Gly
ENST00000242152.6:c.157C>G	ENSP00000242152.2:p.Arg53Gly
ENST00000405982.1:c.157C>G	ENSP00000385282.1:p.Arg53Gly
ENST00000407573.5:c.157C>G	ENSP00000384364.1:p.Arg53Gly
NM_000905.3:c.157C>G	NP_000896.1:p.Arg53Gly
XM_017012910.1:c.42-29698G>C	XP_016868399.1:n.42-29698G>C
XM_017012911.1:c.42-29698G>C	XP_016868400.1:n.42-29698G>C
XR_001745121.1:n.473+33960G>C
XR_001745122.1:n.345-88368G>C
XR_001745123.1:n.473+33960G>C
XR_001745124.1:n.473+33960G>C
XR_001745125.1:n.473+33960G>C
XR_001745126.1:n.473+33960G>C
XR_001745127.1:n.345-29698G>C
XR_001745129.1:n.473+33960G>C
XR_001745130.1:n.473+33960G>C
XR_001745131.1:n.473+33960G>C
XR_001745132.1:n.473+33960G>C
NM_000905.4:c.157C>G MANE Select	NP_000896.1:p.Arg53Gly