Canonical Allele Identifier: CA2565801771
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324689_163324692del , CM000666.2:g.163324689_163324692del GRCh38
NC_000004.11:g.164245841_164245844del , CM000666.1:g.164245841_164245844del GRCh37
NC_000004.10:g.164465291_164465294del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*611_*614del MANE Select ENSP00000354652.2:n.*611_*614del
ENST00000296533.2:c.*611_*614del ENSP00000354652.2:n.*611_*614del
NM_000909.5:c.*611_*614del NP_000900.1:n.*611_*614del
XM_005263031.2:c.*611_*614del XP_005263088.1:n.*611_*614del
XM_011532010.1:c.*611_*614del XP_011530312.1:n.*611_*614del
XM_005263031.4:c.*611_*614del XP_005263088.1:n.*611_*614del
XM_011532010.3:c.*611_*614del XP_011530312.1:n.*611_*614del
NM_000909.6:c.*611_*614del MANE Select NP_000900.1:n.*611_*614del
Search 100 bp 5'
Search 100 bp 3'