Canonical Allele Identifier: CA1505231248

Gene: NPY2R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209650T= , CM000666.2:g.155209650T=	GRCh38
NC_000004.11:g.156130802T= , CM000666.1:g.156130802T=	GRCh37
NC_000004.10:g.156350252T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+581T= MANE Select	ENSP00000332591.3:n.-49+581T=
ENST00000329476.3:c.-49+581T=	ENSP00000332591.3:n.-49+581T=
ENST00000506608.1:c.-49+585T=	ENSP00000426366.1:n.-49+585T=
NM_000910.3:c.-49+581T=	NP_000901.1:n.-49+581T=
XM_005263033.3:c.-48-4242T=	XP_005263090.1:n.-48-4242T=
XM_005263034.3:c.-49+585T=	XP_005263091.1:n.-49+585T=
XM_005263033.4:c.-48-4242T=	XP_005263090.1:n.-48-4242T=
XM_005263034.4:c.-49+585T=	XP_005263091.1:n.-49+585T=
NM_000910.4:c.-49+581T= MANE Select	NP_000901.1:n.-49+581T=
NM_001370180.1:c.-49+585T=	NP_001357109.1:n.-49+585T=
NM_001375470.1:c.-48-4242T=	NP_001362399.1:n.-48-4242T=