Canonical Allele Identifier: CA2774746097

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285128_24285138dup , CM000669.2:g.24285128_24285138dup	GRCh38
NC_000007.13:g.24324747_24324757dup , CM000669.1:g.24324747_24324757dup	GRCh37
NC_000007.12:g.24291272_24291282dup	NCBI36
NG_016148.1:g.5941_5951dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.1-113_1-103dup MANE Select	ENSP00000242152.2:n.1-113_1-103dup
ENST00000242152.6:c.1-113_1-103dup	ENSP00000242152.2:n.1-113_1-103dup
ENST00000405982.1:c.-113_-103dup	ENSP00000385282.1:n.-113_-103dup
ENST00000407573.5:c.-1+52_-1+62dup	ENSP00000384364.1:n.-1+52_-1+62dup
NM_000905.3:c.1-113_1-103dup	NP_000896.1:n.1-113_1-103dup
XM_017012910.1:c.42-29439_42-29429dup	XP_016868399.1:n.42-29439_42-29429dup
XM_017012911.1:c.42-29439_42-29429dup	XP_016868400.1:n.42-29439_42-29429dup
XR_001745121.1:n.473+34219_473+34229dup
XR_001745122.1:n.345-88109_345-88099dup
XR_001745123.1:n.473+34219_473+34229dup
XR_001745124.1:n.473+34219_473+34229dup
XR_001745125.1:n.473+34219_473+34229dup
XR_001745126.1:n.473+34219_473+34229dup
XR_001745127.1:n.345-29439_345-29429dup
XR_001745129.1:n.473+34219_473+34229dup
XR_001745130.1:n.473+34219_473+34229dup
XR_001745131.1:n.473+34219_473+34229dup
XR_001745132.1:n.473+34219_473+34229dup
NM_000905.4:c.1-113_1-103dup MANE Select	NP_000896.1:n.1-113_1-103dup