Canonical Allele Identifier: CA1070340694
Gene: NPY1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324746_163324754dup , CM000666.2:g.163324746_163324754dup GRCh38
NC_000004.11:g.164245898_164245906dup , CM000666.1:g.164245898_164245906dup GRCh37
NC_000004.10:g.164465348_164465356dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*554_*562dup MANE Select ENSP00000354652.2:n.*554_*562dup
ENST00000296533.2:c.*554_*562dup ENSP00000354652.2:n.*554_*562dup
NM_000909.5:c.*554_*562dup NP_000900.1:n.*554_*562dup
XM_005263031.2:c.*554_*562dup XP_005263088.1:n.*554_*562dup
XM_011532010.1:c.*554_*562dup XP_011530312.1:n.*554_*562dup
XM_005263031.4:c.*554_*562dup XP_005263088.1:n.*554_*562dup
XM_011532010.3:c.*554_*562dup XP_011530312.1:n.*554_*562dup
NM_000909.6:c.*554_*562dup MANE Select NP_000900.1:n.*554_*562dup