Canonical Allele Identifier: CA1338049433

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277893G= , CM000664.2:g.238277893G=	GRCh38
NC_000002.11:g.239186534G= , CM000664.1:g.239186534G=	GRCh37
NC_000002.10:g.238851273G=	NCBI36
NG_012146.1:g.15674C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.44C=	ENSP00000516757.1:p.Thr15=
ENST00000707130.1:c.44C=	ENSP00000516758.1:p.Thr15=
ENST00000254657.8:c.44C= MANE Select	ENSP00000254657.3:p.Thr15=
ENST00000254657.7:c.44C=	ENSP00000254657.3:p.Thr15=
ENST00000355768.6:c.44C=	ENSP00000348013.2:p.Thr15=
ENST00000431832.1:c.44C=	ENSP00000405891.1:p.Thr15=
NM_022817.2:c.44C=	NP_073728.1:p.Thr15=
XM_005246111.3:c.44C=	XP_005246168.1:p.Thr15=
XM_006712824.2:c.44C=	XP_006712887.1:p.Thr15=
XM_005246111.4:c.44C=	XP_005246168.1:p.Thr15=
XM_006712824.4:c.44C=	XP_006712887.1:p.Thr15=
NM_022817.3:c.44C= MANE Select	NP_073728.1:p.Thr15=