Canonical Allele Identifier: CA2501908602

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291388C>T , CM000669.2:g.24291388C>T	GRCh38
NC_000007.13:g.24331007C>T , CM000669.1:g.24331007C>T	GRCh37
NC_000007.12:g.24297532C>T	NCBI36
NG_016148.1:g.12201C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.270-275C>T MANE Select	ENSP00000242152.2:n.270-275C>T
ENST00000242152.6:c.270-275C>T	ENSP00000242152.2:n.270-275C>T
ENST00000405982.1:c.270-275C>T	ENSP00000385282.1:n.270-275C>T
ENST00000407573.5:c.270-275C>T	ENSP00000384364.1:n.270-275C>T
NM_000905.3:c.270-275C>T	NP_000896.1:n.270-275C>T
XM_017012910.1:c.41+27969G>A	XP_016868399.1:n.41+27969G>A
XM_017012911.1:c.41+27969G>A	XP_016868400.1:n.41+27969G>A
XR_001745121.1:n.473+27969G>A
XR_001745122.1:n.345-94359G>A
XR_001745123.1:n.473+27969G>A
XR_001745124.1:n.473+27969G>A
XR_001745125.1:n.473+27969G>A
XR_001745126.1:n.473+27969G>A
XR_001745127.1:n.345-35689G>A
XR_001745129.1:n.473+27969G>A
XR_001745130.1:n.473+27969G>A
XR_001745131.1:n.473+27969G>A
XR_001745132.1:n.473+27969G>A
NM_000905.4:c.270-275C>T MANE Select	NP_000896.1:n.270-275C>T