Canonical Allele Identifier: CA454132028

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24331282G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291663G>C , CM000669.2:g.24291663G>C	GRCh38
NC_000007.13:g.24331282G>C , CM000669.1:g.24331282G>C	GRCh37
NC_000007.12:g.24297807G>C	NCBI36
NG_016148.1:g.12476G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270G>C MANE Select	ENSP00000242152.2:p.Arg90=
ENST00000242152.6:c.270G>C	ENSP00000242152.2:p.Arg90=
ENST00000405982.1:c.270G>C	ENSP00000385282.1:p.Arg90=
ENST00000407573.5:c.270G>C	ENSP00000384364.1:p.Arg90=
NM_000905.3:c.270G>C	NP_000896.1:p.Arg90=
XM_017012910.1:c.41+27694C>G	XP_016868399.1:n.41+27694C>G
XM_017012911.1:c.41+27694C>G	XP_016868400.1:n.41+27694C>G
XR_001745121.1:n.473+27694C>G
XR_001745122.1:n.345-94634C>G
XR_001745123.1:n.473+27694C>G
XR_001745124.1:n.473+27694C>G
XR_001745125.1:n.473+27694C>G
XR_001745126.1:n.473+27694C>G
XR_001745127.1:n.345-35964C>G
XR_001745129.1:n.473+27694C>G
XR_001745130.1:n.473+27694C>G
XR_001745131.1:n.473+27694C>G
XR_001745132.1:n.473+27694C>G
NM_000905.4:c.270G>C MANE Select	NP_000896.1:p.Arg90=