Canonical Allele Identifier: CA1509094221
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324589T= , CM000666.2:g.163324589T= GRCh38
NC_000004.11:g.164245741T= , CM000666.1:g.164245741T= GRCh37
NC_000004.10:g.164465191T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296533.3:c.*714A= MANE Select ENSP00000354652.2:n.*714A=
ENST00000296533.2:c.*714A= ENSP00000354652.2:n.*714A=
NM_000909.5:c.*714A= NP_000900.1:n.*714A=
XM_005263031.2:c.*714A= XP_005263088.1:n.*714A=
XM_011532010.1:c.*714A= XP_011530312.1:n.*714A=
XM_005263031.4:c.*714A= XP_005263088.1:n.*714A=
XM_011532010.3:c.*714A= XP_011530312.1:n.*714A=
NM_000909.6:c.*714A= MANE Select NP_000900.1:n.*714A=
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