Canonical Allele Identifier: CA1509094216
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324586_163324587delinsGT , CM000666.2:g.163324586_163324587delinsGT GRCh38
NC_000004.11:g.164245738_164245739delinsGT , CM000666.1:g.164245738_164245739delinsGT GRCh37
NC_000004.10:g.164465188_164465189delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*716_*717delinsAC MANE Select ENSP00000354652.2:n.*716_*717delinsAC
ENST00000296533.2:c.*716_*717delinsAC ENSP00000354652.2:n.*716_*717delinsAC
NM_000909.5:c.*716_*717delinsAC NP_000900.1:n.*716_*717delinsAC
XM_005263031.2:c.*716_*717delinsAC XP_005263088.1:n.*716_*717delinsAC
XM_011532010.1:c.*716_*717delinsAC XP_011530312.1:n.*716_*717delinsAC
XM_005263031.4:c.*716_*717delinsAC XP_005263088.1:n.*716_*717delinsAC
XM_011532010.3:c.*716_*717delinsAC XP_011530312.1:n.*716_*717delinsAC
NM_000909.6:c.*716_*717delinsAC MANE Select NP_000900.1:n.*716_*717delinsAC
Search 100 bp 5'
Search 100 bp 3'