Canonical Allele Identifier: CA1694874167

Gene: NPY

Linked Data

• dbSNP Id: rs1787301834

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24284999C>T , CM000669.2:g.24284999C>T	GRCh38
NC_000007.13:g.24324618C>T , CM000669.1:g.24324618C>T	GRCh37
NC_000007.12:g.24291143C>T	NCBI36
NG_016148.1:g.5812C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-242C>T MANE Select	ENSP00000242152.2:n.1-242C>T
ENST00000242152.6:c.1-242C>T	ENSP00000242152.2:n.1-242C>T
ENST00000407573.5:c.-78C>T	ENSP00000384364.1:n.-78C>T
NM_000905.3:c.1-242C>T	NP_000896.1:n.1-242C>T
XM_017012910.1:c.42-29300G>A	XP_016868399.1:n.42-29300G>A
XM_017012911.1:c.42-29300G>A	XP_016868400.1:n.42-29300G>A
XR_001745121.1:n.473+34358G>A
XR_001745122.1:n.345-87970G>A
XR_001745123.1:n.473+34358G>A
XR_001745124.1:n.473+34358G>A
XR_001745125.1:n.473+34358G>A
XR_001745126.1:n.473+34358G>A
XR_001745127.1:n.345-29300G>A
XR_001745129.1:n.473+34358G>A
XR_001745130.1:n.473+34358G>A
XR_001745131.1:n.473+34358G>A
XR_001745132.1:n.473+34358G>A
NM_000905.4:c.1-242C>T MANE Select	NP_000896.1:n.1-242C>T