Canonical Allele Identifier: CA766699858

Gene: PER2

Linked Data

• dbSNP Id: rs1473760771
• gnomAD v3: 2-238277667-C-CA
• gnomAD v4: 2-238277667-C-CA
• MyVariant Identifiers: chr2:g.239186308_239186309insA (hg19) ; chr2:g.238277667_238277668insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277669dup , CM000664.2:g.238277669dup	GRCh38
NC_000002.11:g.239186310dup , CM000664.1:g.239186310dup	GRCh37
NC_000002.10:g.238851049dup	NCBI36
NG_012146.1:g.15899dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.230+39dup	ENSP00000516757.1:n.230+39dup
ENST00000707130.1:c.230+39dup	ENSP00000516758.1:n.230+39dup
ENST00000254657.8:c.230+39dup MANE Select	ENSP00000254657.3:n.230+39dup
ENST00000254657.7:c.230+39dup	ENSP00000254657.3:n.230+39dup
ENST00000355768.6:c.230+39dup	ENSP00000348013.2:n.230+39dup
ENST00000431832.1:c.230+39dup	ENSP00000405891.1:n.230+39dup
NM_022817.2:c.230+39dup	NP_073728.1:n.230+39dup
XM_005246111.3:c.230+39dup	XP_005246168.1:n.230+39dup
XM_006712824.2:c.230+39dup	XP_006712887.1:n.230+39dup
XM_005246111.4:c.230+39dup	XP_005246168.1:n.230+39dup
XM_006712824.4:c.230+39dup	XP_006712887.1:n.230+39dup
NM_022817.3:c.230+39dup MANE Select	NP_073728.1:n.230+39dup