Canonical Allele Identifier: CA1140186316

Gene: PER3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7837073A= , CM000663.2:g.7837073A=	GRCh38
NC_000001.10:g.7897133A= , CM000663.1:g.7897133A=	GRCh37
NC_000001.9:g.7819720A=	NCBI36
NG_046850.1:g.57694A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377532.8:c.3473A= MANE Select	ENSP00000366755.3:p.His1158=
ENST00000361923.2:c.3446A=	ENSP00000355031.2:p.His1149=
ENST00000377532.7:c.3473A=	ENSP00000366755.3:p.His1158=
ENST00000494684.1:n.266A=
ENST00000613533.4:c.3473A=	ENSP00000482093.1:p.His1158=
ENST00000614998.4:c.3416A=	ENSP00000479223.1:p.His1139=
NM_001289861.1:c.3416A=	NP_001276790.1:p.His1139=
NM_001289862.1:c.3473A=	NP_001276791.1:p.His1158=
NM_001289863.1:c.3395A=	NP_001276792.1:p.His1132=
NM_001289864.1:c.2513A=	NP_001276793.1:p.His838=
NM_016831.2:c.3446A=	NP_058515.1:p.His1149=
XM_005263521.2:c.3470A=	XP_005263578.1:p.His1157=
XM_005263522.2:c.3470A=	XP_005263579.1:p.His1157=
XM_005263523.2:c.3452A=	XP_005263580.1:p.His1151=
XM_005263524.2:c.3473A=	XP_005263581.1:p.His1158=
XM_005263529.2:c.2948A=	XP_005263586.1:p.His983=
XM_011542384.1:c.3473A=	XP_011540686.1:p.His1158=
XM_011542385.1:c.3470A=	XP_011540687.1:p.His1157=
XM_011542386.1:c.3449A=	XP_011540688.1:p.His1150=
XM_011542387.1:c.3305A=	XP_011540689.1:p.His1102=
XM_011542388.1:c.3125A=	XP_011540690.1:p.His1042=
XM_011542389.1:c.3110A=	XP_011540691.1:p.His1037=
XM_011542390.1:c.3449A=	XP_011540692.1:p.His1150=
XM_005263524.4:c.3473A=	XP_005263581.1:p.His1158=
XM_017002723.2:c.3470A=	XP_016858212.1:p.His1157=
XM_017002724.2:c.3467A=	XP_016858213.1:p.His1156=
XM_017002726.2:c.3449A=	XP_016858215.1:p.His1150=
XM_017002727.1:c.3305A=	XP_016858216.1:p.His1102=
XM_017002728.1:c.3125A=	XP_016858217.1:p.His1042=
XM_017002729.1:c.3110A=	XP_016858218.1:p.His1037=
XM_017002730.2:c.3122A=	XP_016858219.1:p.His1041=
XM_017002731.2:c.3101A=	XP_016858220.1:p.His1034=
XM_017002732.1:c.3104A=	XP_016858221.1:p.His1035=
XM_017002733.2:c.2948A=	XP_016858222.1:p.His983=
XM_017002734.1:c.2948A=	XP_016858223.1:p.His983=
XM_017002735.2:c.2945A=	XP_016858224.1:p.His982=
XM_017002737.1:c.2081A=	XP_016858226.1:p.His694=
XM_017002738.2:c.2078A=	XP_016858227.1:p.His693=
XM_024450585.1:c.3473A=	XP_024306353.1:p.His1158=
XM_024450586.1:c.3470A=	XP_024306354.1:p.His1157=
XM_024450587.1:c.3452A=	XP_024306355.1:p.His1151=
XM_024450588.1:c.3449A=	XP_024306356.1:p.His1150=
XM_024450590.1:c.3446A=	XP_024306358.1:p.His1149=
XM_024450611.1:c.2927A=	XP_024306379.1:p.His976=
XM_024450612.1:c.2924A=	XP_024306380.1:p.His975=
NM_001289861.2:c.3416A=	NP_001276790.1:p.His1139=
NM_001289862.2:c.3473A=	NP_001276791.1:p.His1158=
NM_001289863.3:c.3395A=	NP_001276792.1:p.His1132=
NM_001289864.3:c.2513A=	NP_001276793.1:p.His838=
NM_001377275.1:c.3473A= MANE Select	NP_001364204.1:p.His1158=
NM_001377276.1:c.3449A=	NP_001364205.1:p.His1150=
NM_016831.4:c.3446A=	NP_058515.1:p.His1149=