Canonical Allele Identifier: CA1694876924

Gene: NPY

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24290757_24290759delinsTTA , CM000669.2:g.24290757_24290759delinsTTA	GRCh38
NC_000007.13:g.24330376_24330378delinsTTA , CM000669.1:g.24330376_24330378delinsTTA	GRCh37
NC_000007.12:g.24296901_24296903delinsTTA	NCBI36
NG_016148.1:g.11570_11572delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242152.7:c.270-906_270-904delinsTTA MANE Select	ENSP00000242152.2:n.270-906_270-904delinsTTA
ENST00000242152.6:c.270-906_270-904delinsTTA	ENSP00000242152.2:n.270-906_270-904delinsTTA
ENST00000405982.1:c.270-906_270-904delinsTTA	ENSP00000385282.1:n.270-906_270-904delinsTTA
ENST00000407573.5:c.270-906_270-904delinsTTA	ENSP00000384364.1:n.270-906_270-904delinsTTA
NM_000905.3:c.270-906_270-904delinsTTA	NP_000896.1:n.270-906_270-904delinsTTA
XM_017012910.1:c.41+28598_41+28600delinsTAA	XP_016868399.1:n.41+28598_41+28600delinsTAA
XM_017012911.1:c.41+28598_41+28600delinsTAA	XP_016868400.1:n.41+28598_41+28600delinsTAA
XR_001745121.1:n.473+28598_473+28600delinsTAA
XR_001745122.1:n.345-93730_345-93728delinsTAA
XR_001745123.1:n.473+28598_473+28600delinsTAA
XR_001745124.1:n.473+28598_473+28600delinsTAA
XR_001745125.1:n.473+28598_473+28600delinsTAA
XR_001745126.1:n.473+28598_473+28600delinsTAA
XR_001745127.1:n.345-35060_345-35058delinsTAA
XR_001745129.1:n.473+28598_473+28600delinsTAA
XR_001745130.1:n.473+28598_473+28600delinsTAA
XR_001745131.1:n.473+28598_473+28600delinsTAA
XR_001745132.1:n.473+28598_473+28600delinsTAA
NM_000905.4:c.270-906_270-904delinsTTA MANE Select	NP_000896.1:n.270-906_270-904delinsTTA