Canonical Allele Identifier: CA917964826
Gene: NPY HGNC NCBI

Linked Data

dbSNP Id: rs1380194714

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290774_24290775insTATAATTAT , CM000669.2:g.24290774_24290775insTATAATTAT GRCh38
NC_000007.13:g.24330393_24330394insTATAATTAT , CM000669.1:g.24330393_24330394insTATAATTAT GRCh37
NC_000007.12:g.24296918_24296919insTATAATTAT NCBI36
NG_016148.1:g.11587_11588insTATAATTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.7:c.270-889_270-888insTATAATTAT MANE Select ENSP00000242152.2:n.270-889_270-888insTATAATTAT
ENST00000242152.6:c.270-889_270-888insTATAATTAT ENSP00000242152.2:n.270-889_270-888insTATAATTAT
ENST00000405982.1:c.270-889_270-888insTATAATTAT ENSP00000385282.1:n.270-889_270-888insTATAATTAT
ENST00000407573.5:c.270-889_270-888insTATAATTAT ENSP00000384364.1:n.270-889_270-888insTATAATTAT
NM_000905.3:c.270-889_270-888insTATAATTAT NP_000896.1:n.270-889_270-888insTATAATTAT
XM_017012910.1:c.41+28584_41+28585insAATTATAAT XP_016868399.1:n.41+28584_41+28585insAATTATAAT
XM_017012911.1:c.41+28584_41+28585insAATTATAAT XP_016868400.1:n.41+28584_41+28585insAATTATAAT
XR_001745121.1:n.473+28584_473+28585insAATTATAAT
XR_001745122.1:n.345-93744_345-93743insAATTATAAT
XR_001745123.1:n.473+28584_473+28585insAATTATAAT
XR_001745124.1:n.473+28584_473+28585insAATTATAAT
XR_001745125.1:n.473+28584_473+28585insAATTATAAT
XR_001745126.1:n.473+28584_473+28585insAATTATAAT
XR_001745127.1:n.345-35074_345-35073insAATTATAAT
XR_001745129.1:n.473+28584_473+28585insAATTATAAT
XR_001745130.1:n.473+28584_473+28585insAATTATAAT
XR_001745131.1:n.473+28584_473+28585insAATTATAAT
XR_001745132.1:n.473+28584_473+28585insAATTATAAT
NM_000905.4:c.270-889_270-888insTATAATTAT MANE Select NP_000896.1:n.270-889_270-888insTATAATTAT