Canonical Allele Identifier: CA338134189

Gene: PER3

Linked Data

• MyVariant Identifiers: chr1:g.7863202T>C (hg19) ; chr1:g.7803142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7803142T>C , CM000663.2:g.7803142T>C	GRCh38
NC_000001.10:g.7863202T>C , CM000663.1:g.7863202T>C	GRCh37
NC_000001.9:g.7785789T>C	NCBI36
NG_046850.1:g.23763T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377532.8:c.968T>C MANE Select	ENSP00000366755.3:p.Ile323Thr
ENST00000361923.2:c.965T>C	ENSP00000355031.2:p.Ile322Thr
ENST00000377532.7:c.968T>C	ENSP00000366755.3:p.Ile323Thr
ENST00000377541.5:c.965T>C	ENSP00000366764.1:p.Ile322Thr
ENST00000463106.1:n.92T>C
ENST00000613533.4:c.968T>C	ENSP00000482093.1:p.Ile323Thr
ENST00000614998.4:c.968T>C	ENSP00000479223.1:p.Ile323Thr
NM_001289861.1:c.968T>C	NP_001276790.1:p.Ile323Thr
NM_001289862.1:c.968T>C	NP_001276791.1:p.Ile323Thr
NM_001289863.1:c.968T>C	NP_001276792.1:p.Ile323Thr
NM_001289864.1:c.11T>C	NP_001276793.1:p.Ile4Thr
NM_016831.2:c.965T>C	NP_058515.1:p.Ile322Thr
XM_005263521.2:c.968T>C	XP_005263578.1:p.Ile323Thr
XM_005263522.2:c.965T>C	XP_005263579.1:p.Ile322Thr
XM_005263523.2:c.968T>C	XP_005263580.1:p.Ile323Thr
XM_005263524.2:c.968T>C	XP_005263581.1:p.Ile323Thr
XM_005263529.2:c.443T>C	XP_005263586.1:p.Ile148Thr
XM_011542384.1:c.968T>C	XP_011540686.1:p.Ile323Thr
XM_011542385.1:c.968T>C	XP_011540687.1:p.Ile323Thr
XM_011542386.1:c.968T>C	XP_011540688.1:p.Ile323Thr
XM_011542387.1:c.800T>C	XP_011540689.1:p.Ile267Thr
XM_011542388.1:c.620T>C	XP_011540690.1:p.Ile207Thr
XM_011542389.1:c.605T>C	XP_011540691.1:p.Ile202Thr
XM_011542390.1:c.968T>C	XP_011540692.1:p.Ile323Thr
XM_005263524.4:c.968T>C	XP_005263581.1:p.Ile323Thr
XM_017002723.2:c.965T>C	XP_016858212.1:p.Ile322Thr
XM_017002724.2:c.965T>C	XP_016858213.1:p.Ile322Thr
XM_017002726.2:c.965T>C	XP_016858215.1:p.Ile322Thr
XM_017002727.1:c.800T>C	XP_016858216.1:p.Ile267Thr
XM_017002728.1:c.620T>C	XP_016858217.1:p.Ile207Thr
XM_017002729.1:c.605T>C	XP_016858218.1:p.Ile202Thr
XM_017002730.2:c.620T>C	XP_016858219.1:p.Ile207Thr
XM_017002731.2:c.620T>C	XP_016858220.1:p.Ile207Thr
XM_017002732.1:c.620T>C	XP_016858221.1:p.Ile207Thr
XM_017002733.2:c.443T>C	XP_016858222.1:p.Ile148Thr
XM_017002734.1:c.443T>C	XP_016858223.1:p.Ile148Thr
XM_017002735.2:c.443T>C	XP_016858224.1:p.Ile148Thr
XM_017002737.1:c.-298T>C	XP_016858226.1:n.-298T>C
XM_017002738.2:c.-298T>C	XP_016858227.1:n.-298T>C
XM_024450585.1:c.968T>C	XP_024306353.1:p.Ile323Thr
XM_024450586.1:c.968T>C	XP_024306354.1:p.Ile323Thr
XM_024450587.1:c.968T>C	XP_024306355.1:p.Ile323Thr
XM_024450588.1:c.968T>C	XP_024306356.1:p.Ile323Thr
XM_024450590.1:c.965T>C	XP_024306358.1:p.Ile322Thr
XM_024450611.1:c.443T>C	XP_024306379.1:p.Ile148Thr
XM_024450612.1:c.443T>C	XP_024306380.1:p.Ile148Thr
NM_001289861.2:c.968T>C	NP_001276790.1:p.Ile323Thr
NM_001289862.2:c.968T>C	NP_001276791.1:p.Ile323Thr
NM_001289863.3:c.968T>C	NP_001276792.1:p.Ile323Thr
NM_001289864.3:c.11T>C	NP_001276793.1:p.Ile4Thr
NM_001377275.1:c.968T>C MANE Select	NP_001364204.1:p.Ile323Thr
NM_001377276.1:c.968T>C	NP_001364205.1:p.Ile323Thr
NM_016831.4:c.965T>C	NP_058515.1:p.Ile322Thr