Canonical Allele Identifier: CA1505231309

Gene: NPY2R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209775_155209776delinsTG , CM000666.2:g.155209775_155209776delinsTG	GRCh38
NC_000004.11:g.156130927_156130928delinsTG , CM000666.1:g.156130927_156130928delinsTG	GRCh37
NC_000004.10:g.156350377_156350378delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+706_-49+707delinsTG MANE Select	ENSP00000332591.3:n.-49+706_-49+707delinsTG
ENST00000329476.3:c.-49+706_-49+707delinsTG	ENSP00000332591.3:n.-49+706_-49+707delinsTG
ENST00000506608.1:c.-49+710_-49+711delinsTG	ENSP00000426366.1:n.-49+710_-49+711delinsTG
NM_000910.3:c.-49+706_-49+707delinsTG	NP_000901.1:n.-49+706_-49+707delinsTG
XM_005263033.3:c.-48-4117_-48-4116delinsTG	XP_005263090.1:n.-48-4117_-48-4116delinsTG
XM_005263034.3:c.-49+710_-49+711delinsTG	XP_005263091.1:n.-49+710_-49+711delinsTG
XM_005263033.4:c.-48-4117_-48-4116delinsTG	XP_005263090.1:n.-48-4117_-48-4116delinsTG
XM_005263034.4:c.-49+710_-49+711delinsTG	XP_005263091.1:n.-49+710_-49+711delinsTG
NM_000910.4:c.-49+706_-49+707delinsTG MANE Select	NP_000901.1:n.-49+706_-49+707delinsTG
NM_001370180.1:c.-49+710_-49+711delinsTG	NP_001357109.1:n.-49+710_-49+711delinsTG
NM_001375470.1:c.-48-4117_-48-4116delinsTG	NP_001362399.1:n.-48-4117_-48-4116delinsTG