Canonical Allele Identifier: CA789452846

Gene: NPY2R

Linked Data

• dbSNP Id: rs1190400386
• gnomAD v3: 4-155209722-A-AG
• gnomAD v4: 4-155209722-A-AG
• MyVariant Identifiers: chr4:g.156130874_156130875insG (hg19) ; chr4:g.155209722_155209723insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209724dup , CM000666.2:g.155209724dup	GRCh38
NC_000004.11:g.156130876dup , CM000666.1:g.156130876dup	GRCh37
NC_000004.10:g.156350326dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+655dup MANE Select	ENSP00000332591.3:n.-49+655dup
ENST00000329476.3:c.-49+655dup	ENSP00000332591.3:n.-49+655dup
ENST00000506608.1:c.-49+659dup	ENSP00000426366.1:n.-49+659dup
NM_000910.3:c.-49+655dup	NP_000901.1:n.-49+655dup
XM_005263033.3:c.-48-4168dup	XP_005263090.1:n.-48-4168dup
XM_005263034.3:c.-49+659dup	XP_005263091.1:n.-49+659dup
XM_005263033.4:c.-48-4168dup	XP_005263090.1:n.-48-4168dup
XM_005263034.4:c.-49+659dup	XP_005263091.1:n.-49+659dup
NM_000910.4:c.-49+655dup MANE Select	NP_000901.1:n.-49+655dup
NM_001370180.1:c.-49+659dup	NP_001357109.1:n.-49+659dup
NM_001375470.1:c.-48-4168dup	NP_001362399.1:n.-48-4168dup