Canonical Allele Identifier: CA1070340700
Gene: NPY1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324751_163324754del , CM000666.2:g.163324751_163324754del GRCh38
NC_000004.11:g.164245903_164245906del , CM000666.1:g.164245903_164245906del GRCh37
NC_000004.10:g.164465353_164465356del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*559_*562del MANE Select ENSP00000354652.2:n.*559_*562del
ENST00000296533.2:c.*559_*562del ENSP00000354652.2:n.*559_*562del
NM_000909.5:c.*559_*562del NP_000900.1:n.*559_*562del
XM_005263031.2:c.*559_*562del XP_005263088.1:n.*559_*562del
XM_011532010.1:c.*559_*562del XP_011530312.1:n.*559_*562del
XM_005263031.4:c.*559_*562del XP_005263088.1:n.*559_*562del
XM_011532010.3:c.*559_*562del XP_011530312.1:n.*559_*562del
NM_000909.6:c.*559_*562del MANE Select NP_000900.1:n.*559_*562del