Canonical Allele Identifier: CA1509094135

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324514_163324515delinsAT , CM000666.2:g.163324514_163324515delinsAT	GRCh38
NC_000004.11:g.164245666_164245667delinsAT , CM000666.1:g.164245666_164245667delinsAT	GRCh37
NC_000004.10:g.164465116_164465117delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296533.3:c.*788_*789delinsAT MANE Select	ENSP00000354652.2:n.*788_*789delinsAT
ENST00000296533.2:c.*788_*789delinsAT	ENSP00000354652.2:n.*788_*789delinsAT
NM_000909.5:c.*788_*789delinsAT	NP_000900.1:n.*788_*789delinsAT
XM_005263031.2:c.*788_*789delinsAT	XP_005263088.1:n.*788_*789delinsAT
XM_011532010.1:c.*788_*789delinsAT	XP_011530312.1:n.*788_*789delinsAT
XM_005263031.4:c.*788_*789delinsAT	XP_005263088.1:n.*788_*789delinsAT
XM_011532010.3:c.*788_*789delinsAT	XP_011530312.1:n.*788_*789delinsAT
NM_000909.6:c.*788_*789delinsAT MANE Select	NP_000900.1:n.*788_*789delinsAT