Canonical Allele Identifier: CA1509094389

Gene: NPY1R

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.163324740_163324745delinsGAAAAA , CM000666.2:g.163324740_163324745delinsGAAAAA	GRCh38
NC_000004.11:g.164245892_164245897delinsGAAAAA , CM000666.1:g.164245892_164245897delinsGAAAAA	GRCh37
NC_000004.10:g.164465342_164465347delinsGAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296533.3:c.*558_*563delinsTTTTTC MANE Select	ENSP00000354652.2:n.*558_*563delinsTTTTTC
ENST00000296533.2:c.*558_*563delinsTTTTTC	ENSP00000354652.2:n.*558_*563delinsTTTTTC
NM_000909.5:c.*558_*563delinsTTTTTC	NP_000900.1:n.*558_*563delinsTTTTTC
XM_005263031.2:c.*558_*563delinsTTTTTC	XP_005263088.1:n.*558_*563delinsTTTTTC
XM_011532010.1:c.*558_*563delinsTTTTTC	XP_011530312.1:n.*558_*563delinsTTTTTC
XM_005263031.4:c.*558_*563delinsTTTTTC	XP_005263088.1:n.*558_*563delinsTTTTTC
XM_011532010.3:c.*558_*563delinsTTTTTC	XP_011530312.1:n.*558_*563delinsTTTTTC
NM_000909.6:c.*558_*563delinsTTTTTC MANE Select	NP_000900.1:n.*558_*563delinsTTTTTC