Canonical Allele Identifier: CA2839314657

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324646A>C , CM000666.2:g.163324646A>C	GRCh38
NC_000004.11:g.164245798A>C , CM000666.1:g.164245798A>C	GRCh37
NC_000004.10:g.164465248A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296533.3:c.*657T>G MANE Select	ENSP00000354652.2:n.*657T>G
ENST00000296533.2:c.*657T>G	ENSP00000354652.2:n.*657T>G
NM_000909.5:c.*657T>G	NP_000900.1:n.*657T>G
XM_005263031.2:c.*657T>G	XP_005263088.1:n.*657T>G
XM_011532010.1:c.*657T>G	XP_011530312.1:n.*657T>G
XM_005263031.4:c.*657T>G	XP_005263088.1:n.*657T>G
XM_011532010.3:c.*657T>G	XP_011530312.1:n.*657T>G
NM_000909.6:c.*657T>G MANE Select	NP_000900.1:n.*657T>G