Canonical Allele Identifier: CA2764320509

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324671T>C , CM000666.2:g.163324671T>C	GRCh38
NC_000004.11:g.164245823T>C , CM000666.1:g.164245823T>C	GRCh37
NC_000004.10:g.164465273T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*632A>G MANE Select	ENSP00000354652.2:n.*632A>G
ENST00000296533.2:c.*632A>G	ENSP00000354652.2:n.*632A>G
NM_000909.5:c.*632A>G	NP_000900.1:n.*632A>G
XM_005263031.2:c.*632A>G	XP_005263088.1:n.*632A>G
XM_011532010.1:c.*632A>G	XP_011530312.1:n.*632A>G
XM_005263031.4:c.*632A>G	XP_005263088.1:n.*632A>G
XM_011532010.3:c.*632A>G	XP_011530312.1:n.*632A>G
NM_000909.6:c.*632A>G MANE Select	NP_000900.1:n.*632A>G