Canonical Allele Identifier: CA2663914785

Gene: PER2

Linked Data

• gnomAD v4: 2-238256809-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238256810dup , CM000664.2:g.238256810dup	GRCh38
NC_000002.11:g.239165451dup , CM000664.1:g.239165451dup	GRCh37
NC_000002.10:g.238830190dup	NCBI36
NG_012146.1:g.36757dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.2065+112dup	ENSP00000516757.1:n.2065+112dup
ENST00000707130.1:c.2065+112dup	ENSP00000516758.1:n.2065+112dup
ENST00000254657.8:c.2065+112dup MANE Select	ENSP00000254657.3:n.2065+112dup
ENST00000254657.7:c.2065+112dup	ENSP00000254657.3:n.2065+112dup
NM_022817.2:c.2065+112dup	NP_073728.1:n.2065+112dup
XM_005246111.3:c.2065+112dup	XP_005246168.1:n.2065+112dup
XM_006712824.2:c.2065+112dup	XP_006712887.1:n.2065+112dup
XM_005246111.4:c.2065+112dup	XP_005246168.1:n.2065+112dup
XM_006712824.4:c.2065+112dup	XP_006712887.1:n.2065+112dup
NM_022817.3:c.2065+112dup MANE Select	NP_073728.1:n.2065+112dup