Canonical Allele Identifier: CA2672548322
Gene: NPY1R HGNC NCBI

Linked Data

gnomAD v4: 4-163324682-TTTAAATTTTCATTTAAGTGACAATCAGTTGGGAGCAAA-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324689_163324726del , CM000666.2:g.163324689_163324726del GRCh38
NC_000004.11:g.164245841_164245878del , CM000666.1:g.164245841_164245878del GRCh37
NC_000004.10:g.164465291_164465328del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*583_*620del MANE Select ENSP00000354652.2:n.*583_*620del
ENST00000296533.2:c.*583_*620del ENSP00000354652.2:n.*583_*620del
NM_000909.5:c.*583_*620del NP_000900.1:n.*583_*620del
XM_005263031.2:c.*583_*620del XP_005263088.1:n.*583_*620del
XM_011532010.1:c.*583_*620del XP_011530312.1:n.*583_*620del
XM_005263031.4:c.*583_*620del XP_005263088.1:n.*583_*620del
XM_011532010.3:c.*583_*620del XP_011530312.1:n.*583_*620del
NM_000909.6:c.*583_*620del MANE Select NP_000900.1:n.*583_*620del
Search 100 bp 5'
Search 100 bp 3'