Canonical Allele Identifier: CA1509094372
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324734_163324735delinsTA , CM000666.2:g.163324734_163324735delinsTA GRCh38
NC_000004.11:g.164245886_164245887delinsTA , CM000666.1:g.164245886_164245887delinsTA GRCh37
NC_000004.10:g.164465336_164465337delinsTA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*568_*569delinsTA MANE Select ENSP00000354652.2:n.*568_*569delinsTA
ENST00000296533.2:c.*568_*569delinsTA ENSP00000354652.2:n.*568_*569delinsTA
NM_000909.5:c.*568_*569delinsTA NP_000900.1:n.*568_*569delinsTA
XM_005263031.2:c.*568_*569delinsTA XP_005263088.1:n.*568_*569delinsTA
XM_011532010.1:c.*568_*569delinsTA XP_011530312.1:n.*568_*569delinsTA
XM_005263031.4:c.*568_*569delinsTA XP_005263088.1:n.*568_*569delinsTA
XM_011532010.3:c.*568_*569delinsTA XP_011530312.1:n.*568_*569delinsTA
NM_000909.6:c.*568_*569delinsTA MANE Select NP_000900.1:n.*568_*569delinsTA
Search 100 bp 5'
Search 100 bp 3'