Canonical Allele Identifier: CA1509094212
Gene: NPY1R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.163324576T= , CM000666.2:g.163324576T= GRCh38
NC_000004.11:g.164245728T= , CM000666.1:g.164245728T= GRCh37
NC_000004.10:g.164465178T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296533.3:c.*727A= MANE Select ENSP00000354652.2:n.*727A=
ENST00000296533.2:c.*727A= ENSP00000354652.2:n.*727A=
NM_000909.5:c.*727A= NP_000900.1:n.*727A=
XM_005263031.2:c.*727A= XP_005263088.1:n.*727A=
XM_011532010.1:c.*727A= XP_011530312.1:n.*727A=
XM_005263031.4:c.*727A= XP_005263088.1:n.*727A=
XM_011532010.3:c.*727A= XP_011530312.1:n.*727A=
NM_000909.6:c.*727A= MANE Select NP_000900.1:n.*727A=
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