Canonical Allele Identifier: CA1505231292
Gene: NPY2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209731C= , CM000666.2:g.155209731C= GRCh38
NC_000004.11:g.156130883C= , CM000666.1:g.156130883C= GRCh37
NC_000004.10:g.156350333C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329476.4:c.-49+662C= MANE Select ENSP00000332591.3:n.-49+662C=
ENST00000329476.3:c.-49+662C= ENSP00000332591.3:n.-49+662C=
ENST00000506608.1:c.-49+666C= ENSP00000426366.1:n.-49+666C=
NM_000910.3:c.-49+662C= NP_000901.1:n.-49+662C=
XM_005263033.3:c.-48-4161C= XP_005263090.1:n.-48-4161C=
XM_005263034.3:c.-49+666C= XP_005263091.1:n.-49+666C=
XM_005263033.4:c.-48-4161C= XP_005263090.1:n.-48-4161C=
XM_005263034.4:c.-49+666C= XP_005263091.1:n.-49+666C=
NM_000910.4:c.-49+662C= MANE Select NP_000901.1:n.-49+662C=
NM_001370180.1:c.-49+666C= NP_001357109.1:n.-49+666C=
NM_001375470.1:c.-48-4161C= NP_001362399.1:n.-48-4161C=
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