Canonical Allele Identifier: CA1505231313
Gene: NPY2R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.155209781A= , CM000666.2:g.155209781A= GRCh38
NC_000004.11:g.156130933A= , CM000666.1:g.156130933A= GRCh37
NC_000004.10:g.156350383A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000329476.4:c.-49+712A= MANE Select ENSP00000332591.3:n.-49+712A=
ENST00000329476.3:c.-49+712A= ENSP00000332591.3:n.-49+712A=
ENST00000506608.1:c.-49+716A= ENSP00000426366.1:n.-49+716A=
NM_000910.3:c.-49+712A= NP_000901.1:n.-49+712A=
XM_005263033.3:c.-48-4111A= XP_005263090.1:n.-48-4111A=
XM_005263034.3:c.-49+716A= XP_005263091.1:n.-49+716A=
XM_005263033.4:c.-48-4111A= XP_005263090.1:n.-48-4111A=
XM_005263034.4:c.-49+716A= XP_005263091.1:n.-49+716A=
NM_000910.4:c.-49+712A= MANE Select NP_000901.1:n.-49+712A=
NM_001370180.1:c.-49+716A= NP_001357109.1:n.-49+716A=
NM_001375470.1:c.-48-4111A= NP_001362399.1:n.-48-4111A=
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