Canonical Allele Identifier: CA1505231214

Gene: NPY2R

Linked Data

• dbSNP Id: rs1729359591

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209596_155209597del , CM000666.2:g.155209596_155209597del	GRCh38
NC_000004.11:g.156130748_156130749del , CM000666.1:g.156130748_156130749del	GRCh37
NC_000004.10:g.156350198_156350199del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+527_-49+528del MANE Select	ENSP00000332591.3:n.-49+527_-49+528del
ENST00000329476.3:c.-49+527_-49+528del	ENSP00000332591.3:n.-49+527_-49+528del
ENST00000506608.1:c.-49+531_-49+532del	ENSP00000426366.1:n.-49+531_-49+532del
NM_000910.3:c.-49+527_-49+528del	NP_000901.1:n.-49+527_-49+528del
XM_005263033.3:c.-48-4296_-48-4295del	XP_005263090.1:n.-48-4296_-48-4295del
XM_005263034.3:c.-49+531_-49+532del	XP_005263091.1:n.-49+531_-49+532del
XM_005263033.4:c.-48-4296_-48-4295del	XP_005263090.1:n.-48-4296_-48-4295del
XM_005263034.4:c.-49+531_-49+532del	XP_005263091.1:n.-49+531_-49+532del
NM_000910.4:c.-49+527_-49+528del MANE Select	NP_000901.1:n.-49+527_-49+528del
NM_001370180.1:c.-49+531_-49+532del	NP_001357109.1:n.-49+531_-49+532del
NM_001375470.1:c.-48-4296_-48-4295del	NP_001362399.1:n.-48-4296_-48-4295del