Canonical Allele Identifier: CA1509094293

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324648_163324649delinsAT , CM000666.2:g.163324648_163324649delinsAT	GRCh38
NC_000004.11:g.164245800_164245801delinsAT , CM000666.1:g.164245800_164245801delinsAT	GRCh37
NC_000004.10:g.164465250_164465251delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*654_*655delinsAT MANE Select	ENSP00000354652.2:n.*654_*655delinsAT
ENST00000296533.2:c.*654_*655delinsAT	ENSP00000354652.2:n.*654_*655delinsAT
NM_000909.5:c.*654_*655delinsAT	NP_000900.1:n.*654_*655delinsAT
XM_005263031.2:c.*654_*655delinsAT	XP_005263088.1:n.*654_*655delinsAT
XM_011532010.1:c.*654_*655delinsAT	XP_011530312.1:n.*654_*655delinsAT
XM_005263031.4:c.*654_*655delinsAT	XP_005263088.1:n.*654_*655delinsAT
XM_011532010.3:c.*654_*655delinsAT	XP_011530312.1:n.*654_*655delinsAT
NM_000909.6:c.*654_*655delinsAT MANE Select	NP_000900.1:n.*654_*655delinsAT