Canonical Allele Identifier: CA1509094473
Gene: NPY1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324758_163324759delinsAC , CM000666.2:g.163324758_163324759delinsAC GRCh38
NC_000004.11:g.164245910_164245911delinsAC , CM000666.1:g.164245910_164245911delinsAC GRCh37
NC_000004.10:g.164465360_164465361delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*544_*545delinsGT MANE Select ENSP00000354652.2:n.*544_*545delinsGT
ENST00000296533.2:c.*544_*545delinsGT ENSP00000354652.2:n.*544_*545delinsGT
NM_000909.5:c.*544_*545delinsGT NP_000900.1:n.*544_*545delinsGT
XM_005263031.2:c.*544_*545delinsGT XP_005263088.1:n.*544_*545delinsGT
XM_011532010.1:c.*544_*545delinsGT XP_011530312.1:n.*544_*545delinsGT
XM_005263031.4:c.*544_*545delinsGT XP_005263088.1:n.*544_*545delinsGT
XM_011532010.3:c.*544_*545delinsGT XP_011530312.1:n.*544_*545delinsGT
NM_000909.6:c.*544_*545delinsGT MANE Select NP_000900.1:n.*544_*545delinsGT