Canonical Allele Identifier: CA836922731

Gene: NPY

Linked Data

• dbSNP Id: rs1435859342
• MyVariant Identifiers: chr7:g.24324675A>C (hg19) ; chr7:g.24285056A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285056A>C , CM000669.2:g.24285056A>C	GRCh38
NC_000007.13:g.24324675A>C , CM000669.1:g.24324675A>C	GRCh37
NC_000007.12:g.24291200A>C	NCBI36
NG_016148.1:g.5869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-185A>C MANE Select	ENSP00000242152.2:n.1-185A>C
ENST00000242152.6:c.1-185A>C	ENSP00000242152.2:n.1-185A>C
ENST00000407573.5:c.-21A>C	ENSP00000384364.1:n.-21A>C
NM_000905.3:c.1-185A>C	NP_000896.1:n.1-185A>C
XM_017012910.1:c.42-29357T>G	XP_016868399.1:n.42-29357T>G
XM_017012911.1:c.42-29357T>G	XP_016868400.1:n.42-29357T>G
XR_001745121.1:n.473+34301T>G
XR_001745122.1:n.345-88027T>G
XR_001745123.1:n.473+34301T>G
XR_001745124.1:n.473+34301T>G
XR_001745125.1:n.473+34301T>G
XR_001745126.1:n.473+34301T>G
XR_001745127.1:n.345-29357T>G
XR_001745129.1:n.473+34301T>G
XR_001745130.1:n.473+34301T>G
XR_001745131.1:n.473+34301T>G
XR_001745132.1:n.473+34301T>G
NM_000905.4:c.1-185A>C MANE Select	NP_000896.1:n.1-185A>C