Canonical Allele Identifier: CA1509094338

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324702_163324706delinsACAAT , CM000666.2:g.163324702_163324706delinsACAAT	GRCh38
NC_000004.11:g.164245854_164245858delinsACAAT , CM000666.1:g.164245854_164245858delinsACAAT	GRCh37
NC_000004.10:g.164465304_164465308delinsACAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296533.3:c.*597_*601delinsATTGT MANE Select	ENSP00000354652.2:n.*597_*601delinsATTGT
ENST00000296533.2:c.*597_*601delinsATTGT	ENSP00000354652.2:n.*597_*601delinsATTGT
NM_000909.5:c.*597_*601delinsATTGT	NP_000900.1:n.*597_*601delinsATTGT
XM_005263031.2:c.*597_*601delinsATTGT	XP_005263088.1:n.*597_*601delinsATTGT
XM_011532010.1:c.*597_*601delinsATTGT	XP_011530312.1:n.*597_*601delinsATTGT
XM_005263031.4:c.*597_*601delinsATTGT	XP_005263088.1:n.*597_*601delinsATTGT
XM_011532010.3:c.*597_*601delinsATTGT	XP_011530312.1:n.*597_*601delinsATTGT
NM_000909.6:c.*597_*601delinsATTGT MANE Select	NP_000900.1:n.*597_*601delinsATTGT