Canonical Allele Identifier: CA1694877248

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291341_24291342delinsTG , CM000669.2:g.24291341_24291342delinsTG	GRCh38
NC_000007.13:g.24330960_24330961delinsTG , CM000669.1:g.24330960_24330961delinsTG	GRCh37
NC_000007.12:g.24297485_24297486delinsTG	NCBI36
NG_016148.1:g.12154_12155delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000242152.7:c.270-322_270-321delinsTG MANE Select	ENSP00000242152.2:n.270-322_270-321delins...
ENST00000242152.6:c.270-322_270-321delinsTG	ENSP00000242152.2:n.270-322_270-321delins...
ENST00000405982.1:c.270-322_270-321delinsTG	ENSP00000385282.1:n.270-322_270-321delins...
ENST00000407573.5:c.270-322_270-321delinsTG	ENSP00000384364.1:n.270-322_270-321delins...
NM_000905.3:c.270-322_270-321delinsTG	NP_000896.1:n.270-322_270-321delinsTG
XM_017012910.1:c.41+28015_41+28016delinsCA	XP_016868399.1:n.41+28015_41+28016delinsC...
XM_017012911.1:c.41+28015_41+28016delinsCA	XP_016868400.1:n.41+28015_41+28016delinsC...
XR_001745121.1:n.473+28015_473+28016delinsCA
XR_001745122.1:n.345-94313_345-94312delinsCA
XR_001745123.1:n.473+28015_473+28016delinsCA
XR_001745124.1:n.473+28015_473+28016delinsCA
XR_001745125.1:n.473+28015_473+28016delinsCA
XR_001745126.1:n.473+28015_473+28016delinsCA
XR_001745127.1:n.345-35643_345-35642delinsCA
XR_001745129.1:n.473+28015_473+28016delinsCA
XR_001745130.1:n.473+28015_473+28016delinsCA
XR_001745131.1:n.473+28015_473+28016delinsCA
XR_001745132.1:n.473+28015_473+28016delinsCA
NM_000905.4:c.270-322_270-321delinsTG MANE Select	NP_000896.1:n.270-322_270-321delinsTG