Canonical Allele Identifier: CA1338047144
Gene: PER2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238273164A= , CM000664.2:g.238273164A= GRCh38
NC_000002.11:g.239181805A= , CM000664.1:g.239181805A= GRCh37
NC_000002.10:g.238846544A= NCBI36
NG_012146.1:g.20403T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707129.1:c.476T= ENSP00000516757.1:p.Met159=
ENST00000707130.1:c.476T= ENSP00000516758.1:p.Met159=
ENST00000254657.8:c.476T= MANE Select ENSP00000254657.3:p.Met159=
ENST00000254657.7:c.476T= ENSP00000254657.3:p.Met159=
ENST00000355768.6:c.476T= ENSP00000348013.2:p.Met159=
NM_022817.2:c.476T= NP_073728.1:p.Met159=
XM_005246111.3:c.476T= XP_005246168.1:p.Met159=
XM_006712824.2:c.476T= XP_006712887.1:p.Met159=
XM_005246111.4:c.476T= XP_005246168.1:p.Met159=
XM_006712824.4:c.476T= XP_006712887.1:p.Met159=
NM_022817.3:c.476T= MANE Select NP_073728.1:p.Met159=