Canonical Allele Identifier: CA836898586

Gene: NPY

Linked Data

• dbSNP Id: rs1171656416
• gnomAD v3: 7-24291394-T-C
• gnomAD v4: 7-24291394-T-C
• MyVariant Identifiers: chr7:g.24331013T>C (hg19) ; chr7:g.24291394T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291394T>C , CM000669.2:g.24291394T>C	GRCh38
NC_000007.13:g.24331013T>C , CM000669.1:g.24331013T>C	GRCh37
NC_000007.12:g.24297538T>C	NCBI36
NG_016148.1:g.12207T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.270-269T>C MANE Select	ENSP00000242152.2:n.270-269T>C
ENST00000242152.6:c.270-269T>C	ENSP00000242152.2:n.270-269T>C
ENST00000405982.1:c.270-269T>C	ENSP00000385282.1:n.270-269T>C
ENST00000407573.5:c.270-269T>C	ENSP00000384364.1:n.270-269T>C
NM_000905.3:c.270-269T>C	NP_000896.1:n.270-269T>C
XM_017012910.1:c.41+27963A>G	XP_016868399.1:n.41+27963A>G
XM_017012911.1:c.41+27963A>G	XP_016868400.1:n.41+27963A>G
XR_001745121.1:n.473+27963A>G
XR_001745122.1:n.345-94365A>G
XR_001745123.1:n.473+27963A>G
XR_001745124.1:n.473+27963A>G
XR_001745125.1:n.473+27963A>G
XR_001745126.1:n.473+27963A>G
XR_001745127.1:n.345-35695A>G
XR_001745129.1:n.473+27963A>G
XR_001745130.1:n.473+27963A>G
XR_001745131.1:n.473+27963A>G
XR_001745132.1:n.473+27963A>G
NM_000905.4:c.270-269T>C MANE Select	NP_000896.1:n.270-269T>C