Canonical Allele Identifier: CA1099401102
Gene: NPY HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24290790_24290791insATTATGATTATTATT , CM000669.2:g.24290790_24290791insATTATGATTATTATT GRCh38
NC_000007.13:g.24330409_24330410insATTATGATTATTATT , CM000669.1:g.24330409_24330410insATTATGATTATTATT GRCh37
NC_000007.12:g.24296934_24296935insATTATGATTATTATT NCBI36
NG_016148.1:g.11603_11604insATTATGATTATTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000242152.7:c.270-873_270-872insATTATGATTATTATT MANE Select ENSP00000242152.2:n.270-873_270-872insATTATGATTATTATT
ENST00000242152.6:c.270-873_270-872insATTATGATTATTATT ENSP00000242152.2:n.270-873_270-872insATTATGATTATTATT
ENST00000405982.1:c.270-873_270-872insATTATGATTATTATT ENSP00000385282.1:n.270-873_270-872insATTATGATTATTATT
ENST00000407573.5:c.270-873_270-872insATTATGATTATTATT ENSP00000384364.1:n.270-873_270-872insATTATGATTATTATT
NM_000905.3:c.270-873_270-872insATTATGATTATTATT NP_000896.1:n.270-873_270-872insATTATGATTATTATT
XM_017012910.1:c.41+28575_41+28576insCATAATAATAATAAT XP_016868399.1:n.41+28575_41+28576insCATAATAATAATAAT
XM_017012911.1:c.41+28575_41+28576insCATAATAATAATAAT XP_016868400.1:n.41+28575_41+28576insCATAATAATAATAAT
XR_001745121.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745122.1:n.345-93753_345-93752insCATAATAATAATAAT
XR_001745123.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745124.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745125.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745126.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745127.1:n.345-35083_345-35082insCATAATAATAATAAT
XR_001745129.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745130.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745131.1:n.473+28575_473+28576insCATAATAATAATAAT
XR_001745132.1:n.473+28575_473+28576insCATAATAATAATAAT
NM_000905.4:c.270-873_270-872insATTATGATTATTATT MANE Select NP_000896.1:n.270-873_270-872insATTATGATTATTATT