Canonical Allele Identifier: CA1694877466

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24291801_24291803delinsAAT , CM000669.2:g.24291801_24291803delinsAAT	GRCh38
NC_000007.13:g.24331420_24331422delinsAAT , CM000669.1:g.24331420_24331422delinsAAT	GRCh37
NC_000007.12:g.24297945_24297947delinsAAT	NCBI36
NG_016148.1:g.12614_12616delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.*114_*116delinsAAT MANE Select	ENSP00000242152.2:n.*114_*116delinsAAT
ENST00000242152.6:c.*114_*116delinsAAT	ENSP00000242152.2:n.*114_*116delinsAAT
ENST00000405982.1:c.*114_*116delinsAAT	ENSP00000385282.1:n.*114_*116delinsAAT
ENST00000407573.5:c.*114_*116delinsAAT	ENSP00000384364.1:n.*114_*116delinsAAT
NM_000905.3:c.*114_*116delinsAAT	NP_000896.1:n.*114_*116delinsAAT
XM_017012910.1:c.41+27554_41+27556delinsATT	XP_016868399.1:n.41+27554_41+27556delinsATT
XM_017012911.1:c.41+27554_41+27556delinsATT	XP_016868400.1:n.41+27554_41+27556delinsATT
XR_001745121.1:n.473+27554_473+27556delinsATT
XR_001745122.1:n.345-94774_345-94772delinsATT
XR_001745123.1:n.473+27554_473+27556delinsATT
XR_001745124.1:n.473+27554_473+27556delinsATT
XR_001745125.1:n.473+27554_473+27556delinsATT
XR_001745126.1:n.473+27554_473+27556delinsATT
XR_001745127.1:n.345-36104_345-36102delinsATT
XR_001745129.1:n.473+27554_473+27556delinsATT
XR_001745130.1:n.473+27554_473+27556delinsATT
XR_001745131.1:n.473+27554_473+27556delinsATT
XR_001745132.1:n.473+27554_473+27556delinsATT
NM_000905.4:c.*114_*116delinsAAT MANE Select	NP_000896.1:n.*114_*116delinsAAT