Canonical Allele Identifier: CA1338049472

Gene: PER2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238277964_238277966delinsCAG , CM000664.2:g.238277964_238277966delinsCAG	GRCh38
NC_000002.11:g.239186605_239186607delinsCAG , CM000664.1:g.239186605_239186607delinsCAG	GRCh37
NC_000002.10:g.238851344_238851346delinsCAG	NCBI36
NG_012146.1:g.15601_15603delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707129.1:c.-19-11_-19-9delinsCTG	ENSP00000516757.1:n.-19-11_-19-9delinsCTG
ENST00000707130.1:c.-19-11_-19-9delinsCTG	ENSP00000516758.1:n.-19-11_-19-9delinsCTG
ENST00000254657.8:c.-19-11_-19-9delinsCTG MANE Select	ENSP00000254657.3:n.-19-11_-19-9delinsCTG
ENST00000254657.7:c.-19-11_-19-9delinsCTG	ENSP00000254657.3:n.-19-11_-19-9delinsCTG
ENST00000431832.1:c.-19-11_-19-9delinsCTG	ENSP00000405891.1:n.-19-11_-19-9delinsCTG
NM_022817.2:c.-19-11_-19-9delinsCTG	NP_073728.1:n.-19-11_-19-9delinsCTG
XM_005246111.3:c.-19-11_-19-9delinsCTG	XP_005246168.1:n.-19-11_-19-9delinsCTG
XM_006712824.2:c.-19-11_-19-9delinsCTG	XP_006712887.1:n.-19-11_-19-9delinsCTG
XM_005246111.4:c.-19-11_-19-9delinsCTG	XP_005246168.1:n.-19-11_-19-9delinsCTG
XM_006712824.4:c.-19-11_-19-9delinsCTG	XP_006712887.1:n.-19-11_-19-9delinsCTG
NM_022817.3:c.-19-11_-19-9delinsCTG MANE Select	NP_073728.1:n.-19-11_-19-9delinsCTG