Canonical Allele Identifier: CA2701811035

Gene: PER2

Linked Data

• dbSNP Id: rs2106319854

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273213_238273214insAG , CM000664.2:g.238273213_238273214insAG	GRCh38
NC_000002.11:g.239181854_239181855insAG , CM000664.1:g.239181854_239181855insAG	GRCh37
NC_000002.10:g.238846593_238846594insAG	NCBI36
NG_012146.1:g.20353_20354insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-23_449-22insCT	ENSP00000516757.1:n.449-23_449-22insCT
ENST00000707130.1:c.449-23_449-22insCT	ENSP00000516758.1:n.449-23_449-22insCT
ENST00000254657.8:c.449-23_449-22insCT MANE Select	ENSP00000254657.3:n.449-23_449-22insCT
ENST00000254657.7:c.449-23_449-22insCT	ENSP00000254657.3:n.449-23_449-22insCT
ENST00000355768.6:c.449-23_449-22insCT	ENSP00000348013.2:n.449-23_449-22insCT
NM_022817.2:c.449-23_449-22insCT	NP_073728.1:n.449-23_449-22insCT
XM_005246111.3:c.449-23_449-22insCT	XP_005246168.1:n.449-23_449-22insCT
XM_006712824.2:c.449-23_449-22insCT	XP_006712887.1:n.449-23_449-22insCT
XM_005246111.4:c.449-23_449-22insCT	XP_005246168.1:n.449-23_449-22insCT
XM_006712824.4:c.449-23_449-22insCT	XP_006712887.1:n.449-23_449-22insCT
NM_022817.3:c.449-23_449-22insCT MANE Select	NP_073728.1:n.449-23_449-22insCT