Canonical Allele Identifier: CA1152040046

Gene: PER3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7806093C= , CM000663.2:g.7806093C=	GRCh38
NC_000001.10:g.7866153C= , CM000663.1:g.7866153C=	GRCh37
NC_000001.9:g.7788740C=	NCBI36
NG_046850.1:g.26714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377532.8:c.1136+2245C= MANE Select	ENSP00000366755.3:n.1136+2245C=
ENST00000361923.2:c.1133+2245C=	ENSP00000355031.2:n.1133+2245C=
ENST00000377532.7:c.1136+2245C=	ENSP00000366755.3:n.1136+2245C=
ENST00000463106.1:n.260+2245C=
ENST00000613533.4:c.1136+2245C=	ENSP00000482093.1:n.1136+2245C=
ENST00000614998.4:c.1136+2245C=	ENSP00000479223.1:n.1136+2245C=
NM_001289861.1:c.1136+2245C=	NP_001276790.1:n.1136+2245C=
NM_001289862.1:c.1136+2245C=	NP_001276791.1:n.1136+2245C=
NM_001289863.1:c.1136+2245C=	NP_001276792.1:n.1136+2245C=
NM_001289864.1:c.179+2245C=	NP_001276793.1:n.179+2245C=
NM_016831.2:c.1133+2245C=	NP_058515.1:n.1133+2245C=
XM_005263521.2:c.1136+2245C=	XP_005263578.1:n.1136+2245C=
XM_005263522.2:c.1133+2245C=	XP_005263579.1:n.1133+2245C=
XM_005263523.2:c.1136+2245C=	XP_005263580.1:n.1136+2245C=
XM_005263524.2:c.1136+2245C=	XP_005263581.1:n.1136+2245C=
XM_005263529.2:c.611+2245C=	XP_005263586.1:n.611+2245C=
XM_011542384.1:c.1136+2245C=	XP_011540686.1:n.1136+2245C=
XM_011542385.1:c.1136+2245C=	XP_011540687.1:n.1136+2245C=
XM_011542386.1:c.1136+2245C=	XP_011540688.1:n.1136+2245C=
XM_011542387.1:c.968+2245C=	XP_011540689.1:n.968+2245C=
XM_011542388.1:c.788+2245C=	XP_011540690.1:n.788+2245C=
XM_011542389.1:c.773+2245C=	XP_011540691.1:n.773+2245C=
XM_011542390.1:c.1136+2245C=	XP_011540692.1:n.1136+2245C=
XM_005263524.4:c.1136+2245C=	XP_005263581.1:n.1136+2245C=
XM_017002723.2:c.1133+2245C=	XP_016858212.1:n.1133+2245C=
XM_017002724.2:c.1133+2245C=	XP_016858213.1:n.1133+2245C=
XM_017002726.2:c.1133+2245C=	XP_016858215.1:n.1133+2245C=
XM_017002727.1:c.968+2245C=	XP_016858216.1:n.968+2245C=
XM_017002728.1:c.788+2245C=	XP_016858217.1:n.788+2245C=
XM_017002729.1:c.773+2245C=	XP_016858218.1:n.773+2245C=
XM_017002730.2:c.788+2245C=	XP_016858219.1:n.788+2245C=
XM_017002731.2:c.788+2245C=	XP_016858220.1:n.788+2245C=
XM_017002732.1:c.788+2245C=	XP_016858221.1:n.788+2245C=
XM_017002733.2:c.611+2245C=	XP_016858222.1:n.611+2245C=
XM_017002734.1:c.611+2245C=	XP_016858223.1:n.611+2245C=
XM_017002735.2:c.611+2245C=	XP_016858224.1:n.611+2245C=
XM_017002737.1:c.-130+2245C=	XP_016858226.1:n.-130+2245C=
XM_017002738.2:c.-130+2245C=	XP_016858227.1:n.-130+2245C=
XM_024450585.1:c.1136+2245C=	XP_024306353.1:n.1136+2245C=
XM_024450586.1:c.1136+2245C=	XP_024306354.1:n.1136+2245C=
XM_024450587.1:c.1136+2245C=	XP_024306355.1:n.1136+2245C=
XM_024450588.1:c.1136+2245C=	XP_024306356.1:n.1136+2245C=
XM_024450590.1:c.1133+2245C=	XP_024306358.1:n.1133+2245C=
XM_024450611.1:c.611+2245C=	XP_024306379.1:n.611+2245C=
XM_024450612.1:c.611+2245C=	XP_024306380.1:n.611+2245C=
NM_001289861.2:c.1136+2245C=	NP_001276790.1:n.1136+2245C=
NM_001289862.2:c.1136+2245C=	NP_001276791.1:n.1136+2245C=
NM_001289863.3:c.1136+2245C=	NP_001276792.1:n.1136+2245C=
NM_001289864.3:c.179+2245C=	NP_001276793.1:n.179+2245C=
NM_001377275.1:c.1136+2245C= MANE Select	NP_001364204.1:n.1136+2245C=
NM_001377276.1:c.1136+2245C=	NP_001364205.1:n.1136+2245C=
NM_016831.4:c.1133+2245C=	NP_058515.1:n.1133+2245C=