Canonical Allele Identifier: CA67968835

Gene: PER2

Linked Data

• dbSNP Id: rs543506156
• gnomAD v3: 2-238256847-A-AT
• gnomAD v4: 2-238256847-A-AT
• MyVariant Identifiers: chr2:g.239165488_239165489insT (hg19) ; chr2:g.238256847_238256848insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256850dup , CM000664.2:g.238256850dup	GRCh38
NC_000002.11:g.239165491dup , CM000664.1:g.239165491dup	GRCh37
NC_000002.10:g.238830230dup	NCBI36
NG_012146.1:g.36719dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000707129.1:c.2065+74dup	ENSP00000516757.1:n.2065+74dup
ENST00000707130.1:c.2065+74dup	ENSP00000516758.1:n.2065+74dup
ENST00000254657.8:c.2065+74dup MANE Select	ENSP00000254657.3:n.2065+74dup
ENST00000254657.7:c.2065+74dup	ENSP00000254657.3:n.2065+74dup
NM_022817.2:c.2065+74dup	NP_073728.1:n.2065+74dup
XM_005246111.3:c.2065+74dup	XP_005246168.1:n.2065+74dup
XM_006712824.2:c.2065+74dup	XP_006712887.1:n.2065+74dup
XM_005246111.4:c.2065+74dup	XP_005246168.1:n.2065+74dup
XM_006712824.4:c.2065+74dup	XP_006712887.1:n.2065+74dup
NM_022817.3:c.2065+74dup MANE Select	NP_073728.1:n.2065+74dup