Canonical Allele Identifier: CA67985901

Gene: PER2

Linked Data

• dbSNP Id: rs35769430
• MyVariant Identifiers: chr2:g.239181976_239181977insG (hg19) ; chr2:g.238273335_238273336insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273337dup , CM000664.2:g.238273337dup	GRCh38
NC_000002.11:g.239181978dup , CM000664.1:g.239181978dup	GRCh37
NC_000002.10:g.238846717dup	NCBI36
NG_012146.1:g.20231dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-145dup	ENSP00000516757.1:n.449-145dup
ENST00000707130.1:c.449-145dup	ENSP00000516758.1:n.449-145dup
ENST00000254657.8:c.449-145dup MANE Select	ENSP00000254657.3:n.449-145dup
ENST00000254657.7:c.449-145dup	ENSP00000254657.3:n.449-145dup
ENST00000355768.6:c.449-145dup	ENSP00000348013.2:n.449-145dup
NM_022817.2:c.449-145dup	NP_073728.1:n.449-145dup
XM_005246111.3:c.449-145dup	XP_005246168.1:n.449-145dup
XM_006712824.2:c.449-145dup	XP_006712887.1:n.449-145dup
XM_005246111.4:c.449-145dup	XP_005246168.1:n.449-145dup
XM_006712824.4:c.449-145dup	XP_006712887.1:n.449-145dup
NM_022817.3:c.449-145dup MANE Select	NP_073728.1:n.449-145dup