Canonical Allele Identifier: CA2663914811
Gene: PER2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256842_238256843del , CM000664.2:g.238256842_238256843del GRCh38
NC_000002.11:g.239165483_239165484del , CM000664.1:g.239165483_239165484del GRCh37
NC_000002.10:g.238830222_238830223del NCBI36
NG_012146.1:g.36725_36726del

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2065+80_2065+81del ENSP00000516757.1:n.2065+80_2065+81del
ENST00000707130.1:c.2065+80_2065+81del ENSP00000516758.1:n.2065+80_2065+81del
ENST00000254657.8:c.2065+80_2065+81del MANE Select ENSP00000254657.3:n.2065+80_2065+81del
ENST00000254657.7:c.2065+80_2065+81del ENSP00000254657.3:n.2065+80_2065+81del
NM_022817.2:c.2065+80_2065+81del NP_073728.1:n.2065+80_2065+81del
XM_005246111.3:c.2065+80_2065+81del XP_005246168.1:n.2065+80_2065+81del
XM_006712824.2:c.2065+80_2065+81del XP_006712887.1:n.2065+80_2065+81del
XM_005246111.4:c.2065+80_2065+81del XP_005246168.1:n.2065+80_2065+81del
XM_006712824.4:c.2065+80_2065+81del XP_006712887.1:n.2065+80_2065+81del
NM_022817.3:c.2065+80_2065+81del MANE Select NP_073728.1:n.2065+80_2065+81del