Canonical Allele Identifier: CA1509094332
Gene: NPY1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324694T= , CM000666.2:g.163324694T= GRCh38
NC_000004.11:g.164245846T= , CM000666.1:g.164245846T= GRCh37
NC_000004.10:g.164465296T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*609A= MANE Select ENSP00000354652.2:n.*609A=
ENST00000296533.2:c.*609A= ENSP00000354652.2:n.*609A=
NM_000909.5:c.*609A= NP_000900.1:n.*609A=
XM_005263031.2:c.*609A= XP_005263088.1:n.*609A=
XM_011532010.1:c.*609A= XP_011530312.1:n.*609A=
XM_005263031.4:c.*609A= XP_005263088.1:n.*609A=
XM_011532010.3:c.*609A= XP_011530312.1:n.*609A=
NM_000909.6:c.*609A= MANE Select NP_000900.1:n.*609A=