Canonical Allele Identifier: CA1338048514
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238275961G= , CM000664.2:g.238275961G= GRCh38
NC_000002.11:g.239184602G= , CM000664.1:g.239184602G= GRCh37
NC_000002.10:g.238849341G= NCBI36
NG_012146.1:g.17606C=

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.294-64C= ENSP00000516757.1:n.294-64C=
ENST00000707130.1:c.294-64C= ENSP00000516758.1:n.294-64C=
ENST00000254657.8:c.294-64C= MANE Select ENSP00000254657.3:n.294-64C=
ENST00000254657.7:c.294-64C= ENSP00000254657.3:n.294-64C=
ENST00000355768.6:c.294-64C= ENSP00000348013.2:n.294-64C=
ENST00000431832.1:c.294-64C= ENSP00000405891.1:n.294-64C=
NM_022817.2:c.294-64C= NP_073728.1:n.294-64C=
XM_005246111.3:c.294-64C= XP_005246168.1:n.294-64C=
XM_006712824.2:c.294-64C= XP_006712887.1:n.294-64C=
XM_005246111.4:c.294-64C= XP_005246168.1:n.294-64C=
XM_006712824.4:c.294-64C= XP_006712887.1:n.294-64C=
NM_022817.3:c.294-64C= MANE Select NP_073728.1:n.294-64C=