Canonical Allele Identifier: CA1069773494

Gene: NPY2R

Linked Data

• dbSNP Id: rs1322493344
• gnomAD v3: 4-155209778-G-GA
• gnomAD v4: 4-155209778-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209783dup , CM000666.2:g.155209783dup	GRCh38
NC_000004.11:g.156130935dup , CM000666.1:g.156130935dup	GRCh37
NC_000004.10:g.156350385dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+714dup MANE Select	ENSP00000332591.3:n.-49+714dup
ENST00000329476.3:c.-49+714dup	ENSP00000332591.3:n.-49+714dup
ENST00000506608.1:c.-49+718dup	ENSP00000426366.1:n.-49+718dup
NM_000910.3:c.-49+714dup	NP_000901.1:n.-49+714dup
XM_005263033.3:c.-48-4109dup	XP_005263090.1:n.-48-4109dup
XM_005263034.3:c.-49+718dup	XP_005263091.1:n.-49+718dup
XM_005263033.4:c.-48-4109dup	XP_005263090.1:n.-48-4109dup
XM_005263034.4:c.-49+718dup	XP_005263091.1:n.-49+718dup
NM_000910.4:c.-49+714dup MANE Select	NP_000901.1:n.-49+714dup
NM_001370180.1:c.-49+718dup	NP_001357109.1:n.-49+718dup
NM_001375470.1:c.-48-4109dup	NP_001362399.1:n.-48-4109dup