Canonical Allele Identifier: CA1338042103

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238262991G= , CM000664.2:g.238262991G=	GRCh38
NC_000002.11:g.239171632G= , CM000664.1:g.239171632G=	GRCh37
NC_000002.10:g.238836371G=	NCBI36
NG_012146.1:g.30576C=

Transcript Alleles

HGVS	Amino-acid Change
NM_022817.3:c.1114C= MANE Select	NP_073728.1:p.Pro372=
ENST00000254657.8:c.1114C= MANE Select	ENSP00000254657.3:p.Pro372=
NM_022817.2:c.1114C=	NP_073728.1:p.Pro372=
ENST00000254657.7:c.1114C=	ENSP00000254657.3:p.Pro372=
ENST00000355768.6:c.1047-647C=	ENSP00000348013.2:n.1047-647C=
ENST00000707129.1:c.1114C=	ENSP00000516757.1:p.Pro372=
ENST00000707130.1:c.1114C=	ENSP00000516758.1:p.Pro372=
XM_005246111.3:c.1114C=	XP_005246168.1:p.Pro372=
XM_005246111.4:c.1114C=	XP_005246168.1:p.Pro372=
XM_006712824.2:c.1114C=	XP_006712887.1:p.Pro372=
XM_006712824.4:c.1114C=	XP_006712887.1:p.Pro372=