Canonical Allele Identifier: CA2754813330
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238277943del , CM000664.2:g.238277943del GRCh38
NC_000002.11:g.239186584del , CM000664.1:g.239186584del GRCh37
NC_000002.10:g.238851323del NCBI36
NG_012146.1:g.15624del

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.-7del ENSP00000516757.1:n.-7del
ENST00000707130.1:c.-7del ENSP00000516758.1:n.-7del
ENST00000254657.8:c.-7del MANE Select ENSP00000254657.3:n.-7del
ENST00000254657.7:c.-7del ENSP00000254657.3:n.-7del
ENST00000431832.1:c.-7del ENSP00000405891.1:n.-7del
NM_022817.2:c.-7del NP_073728.1:n.-7del
XM_005246111.3:c.-7del XP_005246168.1:n.-7del
XM_006712824.2:c.-7del XP_006712887.1:n.-7del
XM_005246111.4:c.-7del XP_005246168.1:n.-7del
XM_006712824.4:c.-7del XP_006712887.1:n.-7del
NM_022817.3:c.-7del MANE Select NP_073728.1:n.-7del