Canonical Allele Identifier: CA1338047113
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273108_238273111delinsTCTC , CM000664.2:g.238273108_238273111delinsTCTC GRCh38
NC_000002.11:g.239181749_239181752delinsTCTC , CM000664.1:g.239181749_239181752delinsTCTC GRCh37
NC_000002.10:g.238846488_238846491delinsTCTC NCBI36
NG_012146.1:g.20456_20459delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.529_532delinsGAGA ENSP00000516757.1:p.Glu177=
ENST00000707130.1:c.529_532delinsGAGA ENSP00000516758.1:p.Glu177=
ENST00000254657.8:c.529_532delinsGAGA MANE Select ENSP00000254657.3:p.Glu177=
ENST00000254657.7:c.529_532delinsGAGA ENSP00000254657.3:p.Glu177=
ENST00000355768.6:c.529_532delinsGAGA ENSP00000348013.2:p.Glu177=
NM_022817.2:c.529_532delinsGAGA NP_073728.1:p.Glu177=
XM_005246111.3:c.529_532delinsGAGA XP_005246168.1:p.Glu177=
XM_006712824.2:c.529_532delinsGAGA XP_006712887.1:p.Glu177=
XM_005246111.4:c.529_532delinsGAGA XP_005246168.1:p.Glu177=
XM_006712824.4:c.529_532delinsGAGA XP_006712887.1:p.Glu177=
NM_022817.3:c.529_532delinsGAGA MANE Select NP_073728.1:p.Glu177=