Canonical Allele Identifier: CA1694876761
Gene: NPY HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290406_24290428delinsAAACCAAGTTCTACAATGTCAAG , CM000669.2:g.24290406_24290428delinsAAACCAAGTTCTACAATGTCAAG GRCh38
NC_000007.13:g.24330025_24330047delinsAAACCAAGTTCTACAATGTCAAG , CM000669.1:g.24330025_24330047delinsAAACCAAGTTCTACAATGTCAAG GRCh37
NC_000007.12:g.24296550_24296572delinsAAACCAAGTTCTACAATGTCAAG NCBI36
NG_016148.1:g.11219_11241delinsAAACCAAGTTCTACAATGTCAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.7:c.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG MANE Select ENSP00000242152.2:n.269+827_269+849delinsAAACCAAGTTCTACAATGTC...
ENST00000242152.6:c.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG ENSP00000242152.2:n.269+827_269+849delinsAAACCAAGTTCTACAATGTC...
ENST00000405982.1:c.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG ENSP00000385282.1:n.269+827_269+849delinsAAACCAAGTTCTACAATGTC...
ENST00000407573.5:c.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG ENSP00000384364.1:n.269+827_269+849delinsAAACCAAGTTCTACAATGTC...
NM_000905.3:c.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG NP_000896.1:n.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG
XM_017012910.1:c.41+28929_41+28951delinsCTTGACATTGTAGAACTTGGTTT XP_016868399.1:n.41+28929_41+28951delinsCTTGACATTGTAGAACTTGGT...
XM_017012911.1:c.41+28929_41+28951delinsCTTGACATTGTAGAACTTGGTTT XP_016868400.1:n.41+28929_41+28951delinsCTTGACATTGTAGAACTTGGT...
XR_001745121.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745122.1:n.345-93399_345-93377delinsCTTGACATTGTAGAACTTGGTTT
XR_001745123.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745124.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745125.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745126.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745127.1:n.345-34729_345-34707delinsCTTGACATTGTAGAACTTGGTTT
XR_001745129.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745130.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745131.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
XR_001745132.1:n.473+28929_473+28951delinsCTTGACATTGTAGAACTTGGTTT
NM_000905.4:c.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG MANE Select NP_000896.1:n.269+827_269+849delinsAAACCAAGTTCTACAATGTCAAG