Canonical Allele Identifier: CA454132036

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24331294T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291675T>G , CM000669.2:g.24291675T>G	GRCh38
NC_000007.13:g.24331294T>G , CM000669.1:g.24331294T>G	GRCh37
NC_000007.12:g.24297819T>G	NCBI36
NG_016148.1:g.12488T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.282T>G MANE Select	ENSP00000242152.2:p.Pro94=
ENST00000242152.6:c.282T>G	ENSP00000242152.2:p.Pro94=
ENST00000405982.1:c.282T>G	ENSP00000385282.1:p.Pro94=
ENST00000407573.5:c.282T>G	ENSP00000384364.1:p.Pro94=
NM_000905.3:c.282T>G	NP_000896.1:p.Pro94=
XM_017012910.1:c.41+27682A>C	XP_016868399.1:n.41+27682A>C
XM_017012911.1:c.41+27682A>C	XP_016868400.1:n.41+27682A>C
XR_001745121.1:n.473+27682A>C
XR_001745122.1:n.345-94646A>C
XR_001745123.1:n.473+27682A>C
XR_001745124.1:n.473+27682A>C
XR_001745125.1:n.473+27682A>C
XR_001745126.1:n.473+27682A>C
XR_001745127.1:n.345-35976A>C
XR_001745129.1:n.473+27682A>C
XR_001745130.1:n.473+27682A>C
XR_001745131.1:n.473+27682A>C
XR_001745132.1:n.473+27682A>C
NM_000905.4:c.282T>G MANE Select	NP_000896.1:p.Pro94=