Canonical Allele Identifier: CA1139947027

Gene: PER3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7830057T= , CM000663.2:g.7830057T=	GRCh38
NC_000001.10:g.7890117T= , CM000663.1:g.7890117T=	GRCh37
NC_000001.9:g.7812704T=	NCBI36
NG_046850.1:g.50678T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377532.8:c.3110T= MANE Select	ENSP00000366755.3:p.Met1037=
ENST00000361923.2:c.3083T=	ENSP00000355031.2:p.Met1028=
ENST00000377532.7:c.3110T=	ENSP00000366755.3:p.Met1037=
ENST00000613533.4:c.3110T=	ENSP00000482093.1:p.Met1037=
ENST00000614998.4:c.3053T=	ENSP00000479223.1:p.Met1018=
NM_001289861.1:c.3053T=	NP_001276790.1:p.Met1018=
NM_001289862.1:c.3110T=	NP_001276791.1:p.Met1037=
NM_001289863.1:c.3032T=	NP_001276792.1:p.Met1011=
NM_001289864.1:c.2150T=	NP_001276793.1:p.Met717=
NM_016831.2:c.3083T=	NP_058515.1:p.Met1028=
XM_005263521.2:c.3107T=	XP_005263578.1:p.Met1036=
XM_005263522.2:c.3107T=	XP_005263579.1:p.Met1036=
XM_005263523.2:c.3089T=	XP_005263580.1:p.Met1030=
XM_005263524.2:c.3110T=	XP_005263581.1:p.Met1037=
XM_005263529.2:c.2585T=	XP_005263586.1:p.Met862=
XM_011542384.1:c.3110T=	XP_011540686.1:p.Met1037=
XM_011542385.1:c.3107T=	XP_011540687.1:p.Met1036=
XM_011542386.1:c.3086T=	XP_011540688.1:p.Met1029=
XM_011542387.1:c.2942T=	XP_011540689.1:p.Met981=
XM_011542388.1:c.2762T=	XP_011540690.1:p.Met921=
XM_011542389.1:c.2747T=	XP_011540691.1:p.Met916=
XM_011542390.1:c.3086T=	XP_011540692.1:p.Met1029=
XM_005263524.4:c.3110T=	XP_005263581.1:p.Met1037=
XM_017002723.2:c.3107T=	XP_016858212.1:p.Met1036=
XM_017002724.2:c.3104T=	XP_016858213.1:p.Met1035=
XM_017002726.2:c.3086T=	XP_016858215.1:p.Met1029=
XM_017002727.1:c.2942T=	XP_016858216.1:p.Met981=
XM_017002728.1:c.2762T=	XP_016858217.1:p.Met921=
XM_017002729.1:c.2747T=	XP_016858218.1:p.Met916=
XM_017002730.2:c.2759T=	XP_016858219.1:p.Met920=
XM_017002731.2:c.2738T=	XP_016858220.1:p.Met913=
XM_017002732.1:c.2741T=	XP_016858221.1:p.Met914=
XM_017002733.2:c.2585T=	XP_016858222.1:p.Met862=
XM_017002734.1:c.2585T=	XP_016858223.1:p.Met862=
XM_017002735.2:c.2582T=	XP_016858224.1:p.Met861=
XM_017002737.1:c.1718T=	XP_016858226.1:p.Met573=
XM_017002738.2:c.1715T=	XP_016858227.1:p.Met572=
XM_024450585.1:c.3110T=	XP_024306353.1:p.Met1037=
XM_024450586.1:c.3107T=	XP_024306354.1:p.Met1036=
XM_024450587.1:c.3089T=	XP_024306355.1:p.Met1030=
XM_024450588.1:c.3086T=	XP_024306356.1:p.Met1029=
XM_024450590.1:c.3083T=	XP_024306358.1:p.Met1028=
XM_024450611.1:c.2564T=	XP_024306379.1:p.Met855=
XM_024450612.1:c.2561T=	XP_024306380.1:p.Met854=
NM_001289861.2:c.3053T=	NP_001276790.1:p.Met1018=
NM_001289862.2:c.3110T=	NP_001276791.1:p.Met1037=
NM_001289863.3:c.3032T=	NP_001276792.1:p.Met1011=
NM_001289864.3:c.2150T=	NP_001276793.1:p.Met717=
NM_001377275.1:c.3110T= MANE Select	NP_001364204.1:p.Met1037=
NM_001377276.1:c.3086T=	NP_001364205.1:p.Met1029=
NM_016831.4:c.3083T=	NP_058515.1:p.Met1028=