Canonical Allele Identifier: CA1338049504
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238278036_238278037delinsTG , CM000664.2:g.238278036_238278037delinsTG GRCh38
NC_000002.11:g.239186677_239186678delinsTG , CM000664.1:g.239186677_239186678delinsTG GRCh37
NC_000002.10:g.238851416_238851417delinsTG NCBI36
NG_012146.1:g.15530_15531delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.-19-82_-19-81delinsCA ENSP00000516757.1:n.-19-82_-19-81delinsCA
ENST00000707130.1:c.-19-82_-19-81delinsCA ENSP00000516758.1:n.-19-82_-19-81delinsCA
ENST00000254657.8:c.-19-82_-19-81delinsCA MANE Select ENSP00000254657.3:n.-19-82_-19-81delinsCA
ENST00000254657.7:c.-19-82_-19-81delinsCA ENSP00000254657.3:n.-19-82_-19-81delinsCA
ENST00000431832.1:c.-19-82_-19-81delinsCA ENSP00000405891.1:n.-19-82_-19-81delinsCA
NM_022817.2:c.-19-82_-19-81delinsCA NP_073728.1:n.-19-82_-19-81delinsCA
XM_005246111.3:c.-19-82_-19-81delinsCA XP_005246168.1:n.-19-82_-19-81delinsCA
XM_006712824.2:c.-19-82_-19-81delinsCA XP_006712887.1:n.-19-82_-19-81delinsCA
XM_005246111.4:c.-19-82_-19-81delinsCA XP_005246168.1:n.-19-82_-19-81delinsCA
XM_006712824.4:c.-19-82_-19-81delinsCA XP_006712887.1:n.-19-82_-19-81delinsCA
NM_022817.3:c.-19-82_-19-81delinsCA MANE Select NP_073728.1:n.-19-82_-19-81delinsCA