Canonical Allele Identifier: CA1338048525
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238275973_238276097delinsCATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAGATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAG , CM000664.2:g.238275973_238276097delinsCATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAGATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAG GRCh38
NC_000002.11:g.239184614_239184738delinsCATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAGATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAG , CM000664.1:g.239184614_239184738delinsCATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAGATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAG GRCh37
NC_000002.10:g.238849353_238849477delinsCATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAGATTTTCTCAGCCTCGGCTCTAGAGATGTTCTGGTCTGGGTGGCCCTTTGTGGGGCTCTGTAG NCBI36
NG_012146.1:g.17470_17594delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG ENSP00000516757.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGC...
ENST00000707130.1:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG ENSP00000516758.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGC...
ENST00000254657.8:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG MANE Select ENSP00000254657.3:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGC...
ENST00000254657.7:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG ENSP00000254657.3:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGC...
ENST00000355768.6:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG ENSP00000348013.2:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGC...
ENST00000431832.1:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG ENSP00000405891.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGC...
NM_022817.2:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG NP_073728.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCA...
XM_005246111.3:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG XP_005246168.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCAC...
XM_006712824.2:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG XP_006712887.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCAC...
XM_005246111.4:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG XP_005246168.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCAC...
XM_006712824.4:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG XP_006712887.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCAC...
NM_022817.3:c.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATCTACAGAGCCCCACAAAGGGCCACCCAGACCAGAACATCTCTAGAGCCGAGGCTGAGAAAATG MANE Select NP_073728.1:n.294-200_294-76delinsCTACAGAGCCCCACAAAGGGCCACCCA...