Canonical Allele Identifier: CA1338039078
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238256941C= , CM000664.2:g.238256941C= GRCh38
NC_000002.11:g.239165582C= , CM000664.1:g.239165582C= GRCh37
NC_000002.10:g.238830321C= NCBI36
NG_012146.1:g.36626G=

Transcript Alleles

HGVS Amino-acid change
ENST00000707129.1:c.2046G= ENSP00000516757.1:p.Lys682=
ENST00000707130.1:c.2046G= ENSP00000516758.1:p.Lys682=
ENST00000254657.8:c.2046G= MANE Select ENSP00000254657.3:p.Lys682=
ENST00000254657.7:c.2046G= ENSP00000254657.3:p.Lys682=
NM_022817.2:c.2046G= NP_073728.1:p.Lys682=
XM_005246111.3:c.2046G= XP_005246168.1:p.Lys682=
XM_006712824.2:c.2046G= XP_006712887.1:p.Lys682=
XM_005246111.4:c.2046G= XP_005246168.1:p.Lys682=
XM_006712824.4:c.2046G= XP_006712887.1:p.Lys682=
NM_022817.3:c.2046G= MANE Select NP_073728.1:p.Lys682=