Canonical Allele Identifier: CA1505231253

Gene: NPY2R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155209656_155209658delinsATG , CM000666.2:g.155209656_155209658delinsATG	GRCh38
NC_000004.11:g.156130808_156130810delinsATG , CM000666.1:g.156130808_156130810delinsATG	GRCh37
NC_000004.10:g.156350258_156350260delinsATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329476.4:c.-49+587_-49+589delinsATG MANE Select	ENSP00000332591.3:n.-49+587_-49+589delinsATG
ENST00000329476.3:c.-49+587_-49+589delinsATG	ENSP00000332591.3:n.-49+587_-49+589delinsATG
ENST00000506608.1:c.-49+591_-49+593delinsATG	ENSP00000426366.1:n.-49+591_-49+593delinsATG
NM_000910.3:c.-49+587_-49+589delinsATG	NP_000901.1:n.-49+587_-49+589delinsATG
XM_005263033.3:c.-48-4236_-48-4234delinsATG	XP_005263090.1:n.-48-4236_-48-4234delinsATG
XM_005263034.3:c.-49+591_-49+593delinsATG	XP_005263091.1:n.-49+591_-49+593delinsATG
XM_005263033.4:c.-48-4236_-48-4234delinsATG	XP_005263090.1:n.-48-4236_-48-4234delinsATG
XM_005263034.4:c.-49+591_-49+593delinsATG	XP_005263091.1:n.-49+591_-49+593delinsATG
NM_000910.4:c.-49+587_-49+589delinsATG MANE Select	NP_000901.1:n.-49+587_-49+589delinsATG
NM_001370180.1:c.-49+591_-49+593delinsATG	NP_001357109.1:n.-49+591_-49+593delinsATG
NM_001375470.1:c.-48-4236_-48-4234delinsATG	NP_001362399.1:n.-48-4236_-48-4234delinsATG