Canonical Allele Identifier: CA2672548333
Gene: NPY1R HGNC NCBI

Linked Data

gnomAD v4: 4-163324741-A-AG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324741_163324742insG , CM000666.2:g.163324741_163324742insG GRCh38
NC_000004.11:g.164245893_164245894insG , CM000666.1:g.164245893_164245894insG GRCh37
NC_000004.10:g.164465343_164465344insG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*561_*562insC MANE Select ENSP00000354652.2:n.*561_*562insC
ENST00000296533.2:c.*561_*562insC ENSP00000354652.2:n.*561_*562insC
NM_000909.5:c.*561_*562insC NP_000900.1:n.*561_*562insC
XM_005263031.2:c.*561_*562insC XP_005263088.1:n.*561_*562insC
XM_011532010.1:c.*561_*562insC XP_011530312.1:n.*561_*562insC
XM_005263031.4:c.*561_*562insC XP_005263088.1:n.*561_*562insC
XM_011532010.3:c.*561_*562insC XP_011530312.1:n.*561_*562insC
NM_000909.6:c.*561_*562insC MANE Select NP_000900.1:n.*561_*562insC
Search 100 bp 5'
Search 100 bp 3'