Canonical Allele Identifier: CA1509094143

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324516T= , CM000666.2:g.163324516T=	GRCh38
NC_000004.11:g.164245668T= , CM000666.1:g.164245668T=	GRCh37
NC_000004.10:g.164465118T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*787A= MANE Select	ENSP00000354652.2:n.*787A=
ENST00000296533.2:c.*787A=	ENSP00000354652.2:n.*787A=
NM_000909.5:c.*787A=	NP_000900.1:n.*787A=
XM_005263031.2:c.*787A=	XP_005263088.1:n.*787A=
XM_011532010.1:c.*787A=	XP_011530312.1:n.*787A=
XM_005263031.4:c.*787A=	XP_005263088.1:n.*787A=
XM_011532010.3:c.*787A=	XP_011530312.1:n.*787A=
NM_000909.6:c.*787A= MANE Select	NP_000900.1:n.*787A=