Canonical Allele Identifier: CA1505231219

Gene: NPY2R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209600_155209601delinsAC , CM000666.2:g.155209600_155209601delinsAC	GRCh38
NC_000004.11:g.156130752_156130753delinsAC , CM000666.1:g.156130752_156130753delinsAC	GRCh37
NC_000004.10:g.156350202_156350203delinsAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+531_-49+532delinsAC MANE Select	ENSP00000332591.3:n.-49+531_-49+532delinsAC
ENST00000329476.3:c.-49+531_-49+532delinsAC	ENSP00000332591.3:n.-49+531_-49+532delinsAC
ENST00000506608.1:c.-49+535_-49+536delinsAC	ENSP00000426366.1:n.-49+535_-49+536delinsAC
NM_000910.3:c.-49+531_-49+532delinsAC	NP_000901.1:n.-49+531_-49+532delinsAC
XM_005263033.3:c.-48-4292_-48-4291delinsAC	XP_005263090.1:n.-48-4292_-48-4291delinsAC
XM_005263034.3:c.-49+535_-49+536delinsAC	XP_005263091.1:n.-49+535_-49+536delinsAC
XM_005263033.4:c.-48-4292_-48-4291delinsAC	XP_005263090.1:n.-48-4292_-48-4291delinsAC
XM_005263034.4:c.-49+535_-49+536delinsAC	XP_005263091.1:n.-49+535_-49+536delinsAC
NM_000910.4:c.-49+531_-49+532delinsAC MANE Select	NP_000901.1:n.-49+531_-49+532delinsAC
NM_001370180.1:c.-49+535_-49+536delinsAC	NP_001357109.1:n.-49+535_-49+536delinsAC
NM_001375470.1:c.-48-4292_-48-4291delinsAC	NP_001362399.1:n.-48-4292_-48-4291delinsAC