Canonical Allele Identifier: CA1338039091
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256810_238256843delinsTATCGGGCTATGGTGGAGTTCTTCTGCACTTAGA , CM000664.2:g.238256810_238256843delinsTATCGGGCTATGGTGGAGTTCTTCTGCACTTAGA GRCh38
NC_000002.11:g.239165451_239165484delinsTATCGGGCTATGGTGGAGTTCTTCTGCACTTAGA , CM000664.1:g.239165451_239165484delinsTATCGGGCTATGGTGGAGTTCTTCTGCACTTAGA GRCh37
NC_000002.10:g.238830190_238830223delinsTATCGGGCTATGGTGGAGTTCTTCTGCACTTAGA NCBI36
NG_012146.1:g.36724_36757delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA ENSP00000516757.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTC...
ENST00000707130.1:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA ENSP00000516758.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTC...
ENST00000254657.8:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA MANE Select ENSP00000254657.3:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTC...
ENST00000254657.7:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA ENSP00000254657.3:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTC...
NM_022817.2:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA NP_073728.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCAT...
XM_005246111.3:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA XP_005246168.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCAC...
XM_006712824.2:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA XP_006712887.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCAC...
XM_005246111.4:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA XP_005246168.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCAC...
XM_006712824.4:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA XP_006712887.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCAC...
NM_022817.3:c.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCATAGCCCGATA MANE Select NP_073728.1:n.2065+79_2065+112delinsTCTAAGTGCAGAAGAACTCCACCAT...