Canonical Allele Identifier: CA998282565

Gene: PER3

Linked Data

• gnomAD v3: 1-7803415-C-CT
• gnomAD v4: 1-7803415-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7803415_7803416insT , CM000663.2:g.7803415_7803416insT	GRCh38
NC_000001.10:g.7863475_7863476insT , CM000663.1:g.7863475_7863476insT	GRCh37
NC_000001.9:g.7786062_7786063insT	NCBI36
NG_046850.1:g.24036_24037insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377532.8:c.979+262_979+263insT MANE Select	ENSP00000366755.3:n.979+262_979+263insT
ENST00000361923.2:c.976+262_976+263insT	ENSP00000355031.2:n.976+262_976+263insT
ENST00000377532.7:c.979+262_979+263insT	ENSP00000366755.3:n.979+262_979+263insT
ENST00000377541.5:c.976+262_976+263insT	ENSP00000366764.1:n.976+262_976+263insT
ENST00000463106.1:n.103+262_103+263insT
ENST00000613533.4:c.979+262_979+263insT	ENSP00000482093.1:n.979+262_979+263insT
ENST00000614998.4:c.979+262_979+263insT	ENSP00000479223.1:n.979+262_979+263insT
NM_001289861.1:c.979+262_979+263insT	NP_001276790.1:n.979+262_979+263insT
NM_001289862.1:c.979+262_979+263insT	NP_001276791.1:n.979+262_979+263insT
NM_001289863.1:c.979+262_979+263insT	NP_001276792.1:n.979+262_979+263insT
NM_001289864.1:c.22+262_22+263insT	NP_001276793.1:n.22+262_22+263insT
NM_016831.2:c.976+262_976+263insT	NP_058515.1:n.976+262_976+263insT
XM_005263521.2:c.979+262_979+263insT	XP_005263578.1:n.979+262_979+263insT
XM_005263522.2:c.976+262_976+263insT	XP_005263579.1:n.976+262_976+263insT
XM_005263523.2:c.979+262_979+263insT	XP_005263580.1:n.979+262_979+263insT
XM_005263524.2:c.979+262_979+263insT	XP_005263581.1:n.979+262_979+263insT
XM_005263529.2:c.454+262_454+263insT	XP_005263586.1:n.454+262_454+263insT
XM_011542384.1:c.979+262_979+263insT	XP_011540686.1:n.979+262_979+263insT
XM_011542385.1:c.979+262_979+263insT	XP_011540687.1:n.979+262_979+263insT
XM_011542386.1:c.979+262_979+263insT	XP_011540688.1:n.979+262_979+263insT
XM_011542387.1:c.811+262_811+263insT	XP_011540689.1:n.811+262_811+263insT
XM_011542388.1:c.631+262_631+263insT	XP_011540690.1:n.631+262_631+263insT
XM_011542389.1:c.616+262_616+263insT	XP_011540691.1:n.616+262_616+263insT
XM_011542390.1:c.979+262_979+263insT	XP_011540692.1:n.979+262_979+263insT
XM_005263524.4:c.979+262_979+263insT	XP_005263581.1:n.979+262_979+263insT
XM_017002723.2:c.976+262_976+263insT	XP_016858212.1:n.976+262_976+263insT
XM_017002724.2:c.976+262_976+263insT	XP_016858213.1:n.976+262_976+263insT
XM_017002726.2:c.976+262_976+263insT	XP_016858215.1:n.976+262_976+263insT
XM_017002727.1:c.811+262_811+263insT	XP_016858216.1:n.811+262_811+263insT
XM_017002728.1:c.631+262_631+263insT	XP_016858217.1:n.631+262_631+263insT
XM_017002729.1:c.616+262_616+263insT	XP_016858218.1:n.616+262_616+263insT
XM_017002730.2:c.631+262_631+263insT	XP_016858219.1:n.631+262_631+263insT
XM_017002731.2:c.631+262_631+263insT	XP_016858220.1:n.631+262_631+263insT
XM_017002732.1:c.631+262_631+263insT	XP_016858221.1:n.631+262_631+263insT
XM_017002733.2:c.454+262_454+263insT	XP_016858222.1:n.454+262_454+263insT
XM_017002734.1:c.454+262_454+263insT	XP_016858223.1:n.454+262_454+263insT
XM_017002735.2:c.454+262_454+263insT	XP_016858224.1:n.454+262_454+263insT
XM_017002737.1:c.-287+262_-287+263insT	XP_016858226.1:n.-287+262_-287+263insT
XM_017002738.2:c.-287+262_-287+263insT	XP_016858227.1:n.-287+262_-287+263insT
XM_024450585.1:c.979+262_979+263insT	XP_024306353.1:n.979+262_979+263insT
XM_024450586.1:c.979+262_979+263insT	XP_024306354.1:n.979+262_979+263insT
XM_024450587.1:c.979+262_979+263insT	XP_024306355.1:n.979+262_979+263insT
XM_024450588.1:c.979+262_979+263insT	XP_024306356.1:n.979+262_979+263insT
XM_024450590.1:c.976+262_976+263insT	XP_024306358.1:n.976+262_976+263insT
XM_024450611.1:c.454+262_454+263insT	XP_024306379.1:n.454+262_454+263insT
XM_024450612.1:c.454+262_454+263insT	XP_024306380.1:n.454+262_454+263insT
NM_001289861.2:c.979+262_979+263insT	NP_001276790.1:n.979+262_979+263insT
NM_001289862.2:c.979+262_979+263insT	NP_001276791.1:n.979+262_979+263insT
NM_001289863.3:c.979+262_979+263insT	NP_001276792.1:n.979+262_979+263insT
NM_001289864.3:c.22+262_22+263insT	NP_001276793.1:n.22+262_22+263insT
NM_001377275.1:c.979+262_979+263insT MANE Select	NP_001364204.1:n.979+262_979+263insT
NM_001377276.1:c.979+262_979+263insT	NP_001364205.1:n.979+262_979+263insT
NM_016831.4:c.976+262_976+263insT	NP_058515.1:n.976+262_976+263insT