Canonical Allele Identifier: CA1509094170
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324538_163324543delinsTATTAA , CM000666.2:g.163324538_163324543delinsTATTAA GRCh38
NC_000004.11:g.164245690_164245695delinsTATTAA , CM000666.1:g.164245690_164245695delinsTATTAA GRCh37
NC_000004.10:g.164465140_164465145delinsTATTAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*760_*765delinsTTAATA MANE Select ENSP00000354652.2:n.*760_*765delinsTTAATA
ENST00000296533.2:c.*760_*765delinsTTAATA ENSP00000354652.2:n.*760_*765delinsTTAATA
NM_000909.5:c.*760_*765delinsTTAATA NP_000900.1:n.*760_*765delinsTTAATA
XM_005263031.2:c.*760_*765delinsTTAATA XP_005263088.1:n.*760_*765delinsTTAATA
XM_011532010.1:c.*760_*765delinsTTAATA XP_011530312.1:n.*760_*765delinsTTAATA
XM_005263031.4:c.*760_*765delinsTTAATA XP_005263088.1:n.*760_*765delinsTTAATA
XM_011532010.3:c.*760_*765delinsTTAATA XP_011530312.1:n.*760_*765delinsTTAATA
NM_000909.6:c.*760_*765delinsTTAATA MANE Select NP_000900.1:n.*760_*765delinsTTAATA
Search 100 bp 5'
Search 100 bp 3'