Canonical Allele Identifier: CA789452758

Gene: NPY2R

Linked Data

• dbSNP Id: rs1457629681
• MyVariant Identifiers: chr4:g.156130753del (hg19) ; chr4:g.155209601del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209603del , CM000666.2:g.155209603del	GRCh38
NC_000004.11:g.156130755del , CM000666.1:g.156130755del	GRCh37
NC_000004.10:g.156350205del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+534del MANE Select	ENSP00000332591.3:n.-49+534del
ENST00000329476.3:c.-49+534del	ENSP00000332591.3:n.-49+534del
ENST00000506608.1:c.-49+538del	ENSP00000426366.1:n.-49+538del
NM_000910.3:c.-49+534del	NP_000901.1:n.-49+534del
XM_005263033.3:c.-48-4289del	XP_005263090.1:n.-48-4289del
XM_005263034.3:c.-49+538del	XP_005263091.1:n.-49+538del
XM_005263033.4:c.-48-4289del	XP_005263090.1:n.-48-4289del
XM_005263034.4:c.-49+538del	XP_005263091.1:n.-49+538del
NM_000910.4:c.-49+534del MANE Select	NP_000901.1:n.-49+534del
NM_001370180.1:c.-49+538del	NP_001357109.1:n.-49+538del
NM_001375470.1:c.-48-4289del	NP_001362399.1:n.-48-4289del