Canonical Allele Identifier: CA1509094162

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324530_163324535delinsATTTAC , CM000666.2:g.163324530_163324535delinsATTTAC	GRCh38
NC_000004.11:g.164245682_164245687delinsATTTAC , CM000666.1:g.164245682_164245687delinsATTTAC	GRCh37
NC_000004.10:g.164465132_164465137delinsATTTAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296533.3:c.*768_*773delinsGTAAAT MANE Select	ENSP00000354652.2:n.*768_*773delinsGTAAAT
ENST00000296533.2:c.*768_*773delinsGTAAAT	ENSP00000354652.2:n.*768_*773delinsGTAAAT
NM_000909.5:c.*768_*773delinsGTAAAT	NP_000900.1:n.*768_*773delinsGTAAAT
XM_005263031.2:c.*768_*773delinsGTAAAT	XP_005263088.1:n.*768_*773delinsGTAAAT
XM_011532010.1:c.*768_*773delinsGTAAAT	XP_011530312.1:n.*768_*773delinsGTAAAT
XM_005263031.4:c.*768_*773delinsGTAAAT	XP_005263088.1:n.*768_*773delinsGTAAAT
XM_011532010.3:c.*768_*773delinsGTAAAT	XP_011530312.1:n.*768_*773delinsGTAAAT
NM_000909.6:c.*768_*773delinsGTAAAT MANE Select	NP_000900.1:n.*768_*773delinsGTAAAT