Canonical Allele Identifier: CA1070340650
Gene: NPY1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324738_163324740del , CM000666.2:g.163324738_163324740del GRCh38
NC_000004.11:g.164245890_164245892del , CM000666.1:g.164245890_164245892del GRCh37
NC_000004.10:g.164465340_164465342del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*564_*566del MANE Select ENSP00000354652.2:n.*564_*566del
ENST00000296533.2:c.*564_*566del ENSP00000354652.2:n.*564_*566del
NM_000909.5:c.*564_*566del NP_000900.1:n.*564_*566del
XM_005263031.2:c.*564_*566del XP_005263088.1:n.*564_*566del
XM_011532010.1:c.*564_*566del XP_011530312.1:n.*564_*566del
XM_005263031.4:c.*564_*566del XP_005263088.1:n.*564_*566del
XM_011532010.3:c.*564_*566del XP_011530312.1:n.*564_*566del
NM_000909.6:c.*564_*566del MANE Select NP_000900.1:n.*564_*566del