Canonical Allele Identifier: CA1694876977
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290787_24290825delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA , CM000669.2:g.24290787_24290825delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA GRCh38
NC_000007.13:g.24330406_24330444delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA , CM000669.1:g.24330406_24330444delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA GRCh37
NC_000007.12:g.24296931_24296969delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA NCBI36
NG_016148.1:g.11600_11638delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.7:c.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA MANE Select ENSP00000242152.2:n.270-876_270-838delinsTATTCAGAGACAAGGTCTCC...
ENST00000242152.6:c.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA ENSP00000242152.2:n.270-876_270-838delinsTATTCAGAGACAAGGTCTCC...
ENST00000405982.1:c.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA ENSP00000385282.1:n.270-876_270-838delinsTATTCAGAGACAAGGTCTCC...
ENST00000407573.5:c.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA ENSP00000384364.1:n.270-876_270-838delinsTATTCAGAGACAAGGTCTCC...
NM_000905.3:c.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA NP_000896.1:n.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGT...
XM_017012910.1:c.41+28532_41+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA XP_016868399.1:n.41+28532_41+28570delinsTCTGGCCTGAGTGACAGAAGG...
XM_017012911.1:c.41+28532_41+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA XP_016868400.1:n.41+28532_41+28570delinsTCTGGCCTGAGTGACAGAAGG...
XR_001745121.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745122.1:n.345-93796_345-93758delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745123.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745124.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745125.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745126.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745127.1:n.345-35126_345-35088delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745129.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745130.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745131.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
XR_001745132.1:n.473+28532_473+28570delinsTCTGGCCTGAGTGACAGAAGGAGACCTTGTCTCTGAATA
NM_000905.4:c.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGTCACTCAGGCCAGA MANE Select NP_000896.1:n.270-876_270-838delinsTATTCAGAGACAAGGTCTCCTTCTGT...