Canonical Allele Identifier: CA1694874193

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24285035_24285065delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG , CM000669.2:g.24285035_24285065delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG	GRCh38
NC_000007.13:g.24324654_24324684delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG , CM000669.1:g.24324654_24324684delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG	GRCh37
NC_000007.12:g.24291179_24291209delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG	NCBI36
NG_016148.1:g.5848_5878delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG MANE Select	ENSP00000242152.2:n.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACG...
ENST00000242152.6:c.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG	ENSP00000242152.2:n.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACG...
ENST00000407573.5:c.-42_-12delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG	ENSP00000384364.1:n.-42_-12delinsAGAGGGGCAGGTCCCGACCGGACGGCGC...
NM_000905.3:c.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG	NP_000896.1:n.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCC...
XM_017012910.1:c.42-29366_42-29336delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT	XP_016868399.1:n.42-29366_42-29336delinsCGGGCGCCGTCCGGTCGGGAC...
XM_017012911.1:c.42-29366_42-29336delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT	XP_016868400.1:n.42-29366_42-29336delinsCGGGCGCCGTCCGGTCGGGAC...
XR_001745121.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745122.1:n.345-88036_345-88006delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745123.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745124.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745125.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745126.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745127.1:n.345-29366_345-29336delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745129.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745130.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745131.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
XR_001745132.1:n.473+34292_473+34322delinsCGGGCGCCGTCCGGTCGGGACCTGCCCCTCT
NM_000905.4:c.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCCG MANE Select	NP_000896.1:n.1-206_1-176delinsAGAGGGGCAGGTCCCGACCGGACGGCGCCC...