Canonical Allele Identifier: CA1509094227

Gene: NPY1R

Linked Data

• dbSNP Id: rs1734561632

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324596T>C , CM000666.2:g.163324596T>C	GRCh38
NC_000004.11:g.164245748T>C , CM000666.1:g.164245748T>C	GRCh37
NC_000004.10:g.164465198T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*707A>G MANE Select	ENSP00000354652.2:n.*707A>G
ENST00000296533.2:c.*707A>G	ENSP00000354652.2:n.*707A>G
NM_000909.5:c.*707A>G	NP_000900.1:n.*707A>G
XM_005263031.2:c.*707A>G	XP_005263088.1:n.*707A>G
XM_011532010.1:c.*707A>G	XP_011530312.1:n.*707A>G
XM_005263031.4:c.*707A>G	XP_005263088.1:n.*707A>G
XM_011532010.3:c.*707A>G	XP_011530312.1:n.*707A>G
NM_000909.6:c.*707A>G MANE Select	NP_000900.1:n.*707A>G