Canonical Allele Identifier: CA2197859

Gene: PER2

Linked Data

• dbSNP Id: rs765561177
• ExAC: 2:239186302 AGAAAACAACCTG / A
• gnomAD v2: 2-239186302-AGAAAACAACCTG-A
• gnomAD v3: 2-238277661-AGAAAACAACCTG-A
• gnomAD v4: 2-238277661-AGAAAACAACCTG-A
• MyVariant Identifiers: chr2:g.239186303_239186314del (hg19) ; chr2:g.238277662_238277673del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277662_238277673del , CM000664.2:g.238277662_238277673del	GRCh38
NC_000002.11:g.239186303_239186314del , CM000664.1:g.239186303_239186314del	GRCh37
NC_000002.10:g.238851042_238851053del	NCBI36
NG_012146.1:g.15894_15905del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.230+34_230+45del	ENSP00000516757.1:n.230+34_230+45del
ENST00000707130.1:c.230+34_230+45del	ENSP00000516758.1:n.230+34_230+45del
ENST00000254657.8:c.230+34_230+45del MANE Select	ENSP00000254657.3:n.230+34_230+45del
ENST00000254657.7:c.230+34_230+45del	ENSP00000254657.3:n.230+34_230+45del
ENST00000355768.6:c.230+34_230+45del	ENSP00000348013.2:n.230+34_230+45del
ENST00000431832.1:c.230+34_230+45del	ENSP00000405891.1:n.230+34_230+45del
NM_022817.2:c.230+34_230+45del	NP_073728.1:n.230+34_230+45del
XM_005246111.3:c.230+34_230+45del	XP_005246168.1:n.230+34_230+45del
XM_006712824.2:c.230+34_230+45del	XP_006712887.1:n.230+34_230+45del
XM_005246111.4:c.230+34_230+45del	XP_005246168.1:n.230+34_230+45del
XM_006712824.4:c.230+34_230+45del	XP_006712887.1:n.230+34_230+45del
NM_022817.3:c.230+34_230+45del MANE Select	NP_073728.1:n.230+34_230+45del