Canonical Allele Identifier: CA2578849000

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291727_24291728del , CM000669.2:g.24291727_24291728del	GRCh38
NC_000007.13:g.24331346_24331347del , CM000669.1:g.24331346_24331347del	GRCh37
NC_000007.12:g.24297871_24297872del	NCBI36
NG_016148.1:g.12540_12541del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*40_*41del MANE Select	ENSP00000242152.2:n.*40_*41del
ENST00000242152.6:c.*40_*41del	ENSP00000242152.2:n.*40_*41del
ENST00000405982.1:c.*40_*41del	ENSP00000385282.1:n.*40_*41del
ENST00000407573.5:c.*40_*41del	ENSP00000384364.1:n.*40_*41del
NM_000905.3:c.*40_*41del	NP_000896.1:n.*40_*41del
XM_017012910.1:c.41+27629_41+27630del	XP_016868399.1:n.41+27629_41+27630del
XM_017012911.1:c.41+27629_41+27630del	XP_016868400.1:n.41+27629_41+27630del
XR_001745121.1:n.473+27629_473+27630del
XR_001745122.1:n.345-94699_345-94698del
XR_001745123.1:n.473+27629_473+27630del
XR_001745124.1:n.473+27629_473+27630del
XR_001745125.1:n.473+27629_473+27630del
XR_001745126.1:n.473+27629_473+27630del
XR_001745127.1:n.345-36029_345-36028del
XR_001745129.1:n.473+27629_473+27630del
XR_001745130.1:n.473+27629_473+27630del
XR_001745131.1:n.473+27629_473+27630del
XR_001745132.1:n.473+27629_473+27630del
NM_000905.4:c.*40_*41del MANE Select	NP_000896.1:n.*40_*41del