Canonical Allele Identifier: CA367052275

Gene: NPY

Linked Data

• MyVariant Identifiers: chr7:g.24331299T>G (hg19) ; chr7:g.24291680T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291680T>G , CM000669.2:g.24291680T>G	GRCh38
NC_000007.13:g.24331299T>G , CM000669.1:g.24331299T>G	GRCh37
NC_000007.12:g.24297824T>G	NCBI36
NG_016148.1:g.12493T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.287T>G MANE Select	ENSP00000242152.2:p.Met96Arg
ENST00000242152.6:c.287T>G	ENSP00000242152.2:p.Met96Arg
ENST00000405982.1:c.287T>G	ENSP00000385282.1:p.Met96Arg
ENST00000407573.5:c.287T>G	ENSP00000384364.1:p.Met96Arg
NM_000905.3:c.287T>G	NP_000896.1:p.Met96Arg
XM_017012910.1:c.41+27677A>C	XP_016868399.1:n.41+27677A>C
XM_017012911.1:c.41+27677A>C	XP_016868400.1:n.41+27677A>C
XR_001745121.1:n.473+27677A>C
XR_001745122.1:n.345-94651A>C
XR_001745123.1:n.473+27677A>C
XR_001745124.1:n.473+27677A>C
XR_001745125.1:n.473+27677A>C
XR_001745126.1:n.473+27677A>C
XR_001745127.1:n.345-35981A>C
XR_001745129.1:n.473+27677A>C
XR_001745130.1:n.473+27677A>C
XR_001745131.1:n.473+27677A>C
XR_001745132.1:n.473+27677A>C
NM_000905.4:c.287T>G MANE Select	NP_000896.1:p.Met96Arg