Canonical Allele Identifier: CA1338047237

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238273360_238273364delinsCACAG , CM000664.2:g.238273360_238273364delinsCACAG	GRCh38
NC_000002.11:g.239182001_239182005delinsCACAG , CM000664.1:g.239182001_239182005delinsCACAG	GRCh37
NC_000002.10:g.238846740_238846744delinsCACAG	NCBI36
NG_012146.1:g.20203_20207delinsCTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.449-173_449-169delinsCTGTG	ENSP00000516757.1:n.449-173_449-169delinsCTGTG
ENST00000707130.1:c.449-173_449-169delinsCTGTG	ENSP00000516758.1:n.449-173_449-169delinsCTGTG
ENST00000254657.8:c.449-173_449-169delinsCTGTG MANE Select	ENSP00000254657.3:n.449-173_449-169delinsCTGTG
ENST00000254657.7:c.449-173_449-169delinsCTGTG	ENSP00000254657.3:n.449-173_449-169delinsCTGTG
ENST00000355768.6:c.449-173_449-169delinsCTGTG	ENSP00000348013.2:n.449-173_449-169delinsCTGTG
NM_022817.2:c.449-173_449-169delinsCTGTG	NP_073728.1:n.449-173_449-169delinsCTGTG
XM_005246111.3:c.449-173_449-169delinsCTGTG	XP_005246168.1:n.449-173_449-169delinsCTGTG
XM_006712824.2:c.449-173_449-169delinsCTGTG	XP_006712887.1:n.449-173_449-169delinsCTGTG
XM_005246111.4:c.449-173_449-169delinsCTGTG	XP_005246168.1:n.449-173_449-169delinsCTGTG
XM_006712824.4:c.449-173_449-169delinsCTGTG	XP_006712887.1:n.449-173_449-169delinsCTGTG
NM_022817.3:c.449-173_449-169delinsCTGTG MANE Select	NP_073728.1:n.449-173_449-169delinsCTGTG