Canonical Allele Identifier: CA1694876979

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290790_24290825delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA , CM000669.2:g.24290790_24290825delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	GRCh38
NC_000007.13:g.24330409_24330444delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA , CM000669.1:g.24330409_24330444delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	GRCh37
NC_000007.12:g.24296934_24296969delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	NCBI36
NG_016148.1:g.11603_11638delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA MANE Select	ENSP00000242152.2:n.270-873_270-838delinsTCAGAGACAAGGTCTCCTTC...
ENST00000242152.6:c.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	ENSP00000242152.2:n.270-873_270-838delinsTCAGAGACAAGGTCTCCTTC...
ENST00000405982.1:c.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	ENSP00000385282.1:n.270-873_270-838delinsTCAGAGACAAGGTCTCCTTC...
ENST00000407573.5:c.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	ENSP00000384364.1:n.270-873_270-838delinsTCAGAGACAAGGTCTCCTTC...
NM_000905.3:c.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA	NP_000896.1:n.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCAC...
XM_017012910.1:c.41+28532_41+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA	XP_016868399.1:n.41+28532_41+28567delinsTCTGGCCTGAGTGACAGAAGG...
XM_017012911.1:c.41+28532_41+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA	XP_016868400.1:n.41+28532_41+28567delinsTCTGGCCTGAGTGACAGAAGG...
XR_001745121.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745122.1:n.345-93796_345-93761delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745123.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745124.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745125.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745126.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745127.1:n.345-35126_345-35091delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745129.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745130.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745131.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
XR_001745132.1:n.473+28532_473+28567delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGA
NM_000905.4:c.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA MANE Select	NP_000896.1:n.270-873_270-838delinsTCAGAGACAAGGTCTCCTTCTGTCAC...