Canonical Allele Identifier: CA1509094228
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324597_163324598delinsAG , CM000666.2:g.163324597_163324598delinsAG GRCh38
NC_000004.11:g.164245749_164245750delinsAG , CM000666.1:g.164245749_164245750delinsAG GRCh37
NC_000004.10:g.164465199_164465200delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*705_*706delinsCT MANE Select ENSP00000354652.2:n.*705_*706delinsCT
ENST00000296533.2:c.*705_*706delinsCT ENSP00000354652.2:n.*705_*706delinsCT
NM_000909.5:c.*705_*706delinsCT NP_000900.1:n.*705_*706delinsCT
XM_005263031.2:c.*705_*706delinsCT XP_005263088.1:n.*705_*706delinsCT
XM_011532010.1:c.*705_*706delinsCT XP_011530312.1:n.*705_*706delinsCT
XM_005263031.4:c.*705_*706delinsCT XP_005263088.1:n.*705_*706delinsCT
XM_011532010.3:c.*705_*706delinsCT XP_011530312.1:n.*705_*706delinsCT
NM_000909.6:c.*705_*706delinsCT MANE Select NP_000900.1:n.*705_*706delinsCT
Search 100 bp 5'
Search 100 bp 3'