Canonical Allele Identifier: CA2754813238

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273271_238273272insCCCAGGCCCAGGCTGTCTGCAGGATCTTCCCATCGTCCTGGGGCAGGATGAGCTTCAGAGGTTCAGTGATGGCCTCCACTTGCGT , CM000664.2:g.238273271_238273272insCCCAGGCCCAGGCTGTCTGCAGGATCTTCCCATCGTCCTGGGGCAGGATGAGCTTCAGAGGTTCAGTGATGGCCTCCACTTGCGT	GRCh38
NC_000002.11:g.239181912_239181913insCCCAGGCCCAGGCTGTCTGCAGGATCTTCCCATCGTCCTGGGGCAGGATGAGCTTCAGAGGTTCAGTGATGGCCTCCACTTGCGT , CM000664.1:g.239181912_239181913insCCCAGGCCCAGGCTGTCTGCAGGATCTTCCCATCGTCCTGGGGCAGGATGAGCTTCAGAGGTTCAGTGATGGCCTCCACTTGCGT	GRCh37
NC_000002.10:g.238846651_238846652insCCCAGGCCCAGGCTGTCTGCAGGATCTTCCCATCGTCCTGGGGCAGGATGAGCTTCAGAGGTTCAGTGATGGCCTCCACTTGCGT	NCBI36
NG_012146.1:g.20295_20296insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	ENSP00000516757.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAAC...
ENST00000707130.1:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	ENSP00000516758.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAAC...
ENST00000254657.8:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG MANE Select	ENSP00000254657.3:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAAC...
ENST00000254657.7:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	ENSP00000254657.3:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAAC...
ENST00000355768.6:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	ENSP00000348013.2:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAAC...
NM_022817.2:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	NP_073728.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGA...
XM_005246111.3:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	XP_005246168.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTC...
XM_006712824.2:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	XP_006712887.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTC...
XM_005246111.4:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	XP_005246168.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTC...
XM_006712824.4:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG	XP_006712887.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTC...
NM_022817.3:c.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGAAGCTCATCCTGCCCCAGGACGATGGGAAGATCCTGCAGACAGCCTGGGCCTGGG MANE Select	NP_073728.1:n.449-81_449-80insACGCAAGTGGAGGCCATCACTGAACCTCTGA...