Canonical Allele Identifier: CA2578848920

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285192G>T , CM000669.2:g.24285192G>T	GRCh38
NC_000007.13:g.24324811G>T , CM000669.1:g.24324811G>T	GRCh37
NC_000007.12:g.24291336G>T	NCBI36
NG_016148.1:g.6005G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-49G>T MANE Select	ENSP00000242152.2:n.1-49G>T
ENST00000242152.6:c.1-49G>T	ENSP00000242152.2:n.1-49G>T
ENST00000405982.1:c.-49G>T	ENSP00000385282.1:n.-49G>T
ENST00000407573.5:c.1-49G>T	ENSP00000384364.1:n.1-49G>T
NM_000905.3:c.1-49G>T	NP_000896.1:n.1-49G>T
XM_017012910.1:c.42-29493C>A	XP_016868399.1:n.42-29493C>A
XM_017012911.1:c.42-29493C>A	XP_016868400.1:n.42-29493C>A
XR_001745121.1:n.473+34165C>A
XR_001745122.1:n.345-88163C>A
XR_001745123.1:n.473+34165C>A
XR_001745124.1:n.473+34165C>A
XR_001745125.1:n.473+34165C>A
XR_001745126.1:n.473+34165C>A
XR_001745127.1:n.345-29493C>A
XR_001745129.1:n.473+34165C>A
XR_001745130.1:n.473+34165C>A
XR_001745131.1:n.473+34165C>A
XR_001745132.1:n.473+34165C>A
NM_000905.4:c.1-49G>T MANE Select	NP_000896.1:n.1-49G>T