Canonical Allele Identifier: CA1694877390

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291645_24291648delinsGCTT , CM000669.2:g.24291645_24291648delinsGCTT	GRCh38
NC_000007.13:g.24331264_24331267delinsGCTT , CM000669.1:g.24331264_24331267delinsGCTT	GRCh37
NC_000007.12:g.24297789_24297792delinsGCTT	NCBI36
NG_016148.1:g.12458_12461delinsGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-18_270-15delinsGCTT MANE Select	ENSP00000242152.2:n.270-18_270-15delinsGCTT
ENST00000242152.6:c.270-18_270-15delinsGCTT	ENSP00000242152.2:n.270-18_270-15delinsGCTT
ENST00000405982.1:c.270-18_270-15delinsGCTT	ENSP00000385282.1:n.270-18_270-15delinsGCTT
ENST00000407573.5:c.270-18_270-15delinsGCTT	ENSP00000384364.1:n.270-18_270-15delinsGCTT
NM_000905.3:c.270-18_270-15delinsGCTT	NP_000896.1:n.270-18_270-15delinsGCTT
XM_017012910.1:c.41+27709_41+27712delinsAAGC	XP_016868399.1:n.41+27709_41+27712delinsAAGC
XM_017012911.1:c.41+27709_41+27712delinsAAGC	XP_016868400.1:n.41+27709_41+27712delinsAAGC
XR_001745121.1:n.473+27709_473+27712delinsAAGC
XR_001745122.1:n.345-94619_345-94616delinsAAGC
XR_001745123.1:n.473+27709_473+27712delinsAAGC
XR_001745124.1:n.473+27709_473+27712delinsAAGC
XR_001745125.1:n.473+27709_473+27712delinsAAGC
XR_001745126.1:n.473+27709_473+27712delinsAAGC
XR_001745127.1:n.345-35949_345-35946delinsAAGC
XR_001745129.1:n.473+27709_473+27712delinsAAGC
XR_001745130.1:n.473+27709_473+27712delinsAAGC
XR_001745131.1:n.473+27709_473+27712delinsAAGC
XR_001745132.1:n.473+27709_473+27712delinsAAGC
NM_000905.4:c.270-18_270-15delinsGCTT MANE Select	NP_000896.1:n.270-18_270-15delinsGCTT