Canonical Allele Identifier: CA2663887015
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273123_238273124dup , CM000664.2:g.238273123_238273124dup GRCh38
NC_000002.11:g.239181764_239181765dup , CM000664.1:g.239181764_239181765dup GRCh37
NC_000002.10:g.238846503_238846504dup NCBI36
NG_012146.1:g.20443_20444dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.516_517dup ENSP00000516757.1:p.Tyr173SerfsTer16
ENST00000707130.1:c.516_517dup ENSP00000516758.1:p.Tyr173SerfsTer16
ENST00000254657.8:c.516_517dup MANE Select ENSP00000254657.3:p.Tyr173SerfsTer16
ENST00000254657.7:c.516_517dup ENSP00000254657.3:p.Tyr173SerfsTer16
ENST00000355768.6:c.516_517dup ENSP00000348013.2:p.Tyr173SerfsTer16
NM_022817.2:c.516_517dup NP_073728.1:p.Tyr173SerfsTer16
XM_005246111.3:c.516_517dup XP_005246168.1:p.Tyr173SerfsTer16
XM_006712824.2:c.516_517dup XP_006712887.1:p.Tyr173SerfsTer16
XM_005246111.4:c.516_517dup XP_005246168.1:p.Tyr173SerfsTer16
XM_006712824.4:c.516_517dup XP_006712887.1:p.Tyr173SerfsTer16
NM_022817.3:c.516_517dup MANE Select NP_073728.1:p.Tyr173SerfsTer16