Canonical Allele Identifier: CA2505503912

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324591G>C , CM000666.2:g.163324591G>C	GRCh38
NC_000004.11:g.164245743G>C , CM000666.1:g.164245743G>C	GRCh37
NC_000004.10:g.164465193G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*712C>G MANE Select	ENSP00000354652.2:n.*712C>G
ENST00000296533.2:c.*712C>G	ENSP00000354652.2:n.*712C>G
NM_000909.5:c.*712C>G	NP_000900.1:n.*712C>G
XM_005263031.2:c.*712C>G	XP_005263088.1:n.*712C>G
XM_011532010.1:c.*712C>G	XP_011530312.1:n.*712C>G
XM_005263031.4:c.*712C>G	XP_005263088.1:n.*712C>G
XM_011532010.3:c.*712C>G	XP_011530312.1:n.*712C>G
NM_000909.6:c.*712C>G MANE Select	NP_000900.1:n.*712C>G