Canonical Allele Identifier: CA2663888862
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238278076_238278077insATT , CM000664.2:g.238278076_238278077insATT GRCh38
NC_000002.11:g.239186717_239186718insATT , CM000664.1:g.239186717_239186718insATT GRCh37
NC_000002.10:g.238851456_238851457insATT NCBI36
NG_012146.1:g.15492_15493insTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.-19-120_-19-119insTAA ENSP00000516757.1:n.-19-120_-19-119insTAA
ENST00000707130.1:c.-19-120_-19-119insTAA ENSP00000516758.1:n.-19-120_-19-119insTAA
ENST00000254657.8:c.-19-120_-19-119insTAA MANE Select ENSP00000254657.3:n.-19-120_-19-119insTAA
ENST00000254657.7:c.-19-120_-19-119insTAA ENSP00000254657.3:n.-19-120_-19-119insTAA
ENST00000431832.1:c.-19-120_-19-119insTAA ENSP00000405891.1:n.-19-120_-19-119insTAA
NM_022817.2:c.-19-120_-19-119insTAA NP_073728.1:n.-19-120_-19-119insTAA
XM_005246111.3:c.-19-120_-19-119insTAA XP_005246168.1:n.-19-120_-19-119insTAA
XM_006712824.2:c.-19-120_-19-119insTAA XP_006712887.1:n.-19-120_-19-119insTAA
XM_005246111.4:c.-19-120_-19-119insTAA XP_005246168.1:n.-19-120_-19-119insTAA
XM_006712824.4:c.-19-120_-19-119insTAA XP_006712887.1:n.-19-120_-19-119insTAA
NM_022817.3:c.-19-120_-19-119insTAA MANE Select NP_073728.1:n.-19-120_-19-119insTAA