Canonical Allele Identifier: CA1509094197
Gene: NPY1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324570G= , CM000666.2:g.163324570G= GRCh38
NC_000004.11:g.164245722G= , CM000666.1:g.164245722G= GRCh37
NC_000004.10:g.164465172G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*733C= MANE Select ENSP00000354652.2:n.*733C=
ENST00000296533.2:c.*733C= ENSP00000354652.2:n.*733C=
NM_000909.5:c.*733C= NP_000900.1:n.*733C=
XM_005263031.2:c.*733C= XP_005263088.1:n.*733C=
XM_011532010.1:c.*733C= XP_011530312.1:n.*733C=
XM_005263031.4:c.*733C= XP_005263088.1:n.*733C=
XM_011532010.3:c.*733C= XP_011530312.1:n.*733C=
NM_000909.6:c.*733C= MANE Select NP_000900.1:n.*733C=