Canonical Allele Identifier: CA1509094411
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324741A= , CM000666.2:g.163324741A= GRCh38
NC_000004.11:g.164245893A= , CM000666.1:g.164245893A= GRCh37
NC_000004.10:g.164465343A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*562T= MANE Select ENSP00000354652.2:n.*562T=
ENST00000296533.2:c.*562T= ENSP00000354652.2:n.*562T=
NM_000909.5:c.*562T= NP_000900.1:n.*562T=
XM_005263031.2:c.*562T= XP_005263088.1:n.*562T=
XM_011532010.1:c.*562T= XP_011530312.1:n.*562T=
XM_005263031.4:c.*562T= XP_005263088.1:n.*562T=
XM_011532010.3:c.*562T= XP_011530312.1:n.*562T=
NM_000909.6:c.*562T= MANE Select NP_000900.1:n.*562T=
Search 100 bp 5'
Search 100 bp 3'