Canonical Allele Identifier: CA645372341

Gene: PER3

Linked Data

• PubMed: PMID:26903630

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.[7809893C>G;7809900A>G] , CM000663.2:g.[7809893C>G;7809900A>G]	GRCh38
NC_000001.10:g.[7869953C>G;7869960A>G] , CM000663.1:g.[7869953C>G;7869960A>G]	GRCh37
NC_000001.9:g.[7792540C>G;7792547A>G]	NCBI36
NG_046850.1:g.[30514C>G;30521A>G]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377532.8:c.[1243C>G;1250A>G] MANE Select	ENSP00000366755.3:p.[Pro415Ala;His417Arg]
ENST00000361923.2:c.[1240C>G;1247A>G]	ENSP00000355031.2:p.[Pro414Ala;His416Arg]
ENST00000377532.7:c.[1243C>G;1250A>G]	ENSP00000366755.3:p.[Pro415Ala;His417Arg]
ENST00000463106.1:n.[261C>G;268A>G]
ENST00000613533.4:c.[1243C>G;1250A>G]	ENSP00000482093.1:p.[Pro415Ala;His417Arg]
ENST00000614998.4:c.[1243C>G;1250A>G]	ENSP00000479223.1:p.[Pro415Ala;His417Arg]
NM_001289861.1:c.[1243C>G;1250A>G]	NP_001276790.1:p.[Pro415Ala;His417Arg]
NM_001289862.1:c.[1243C>G;1250A>G]	NP_001276791.1:p.[Pro415Ala;His417Arg]
NM_001289863.1:c.[1243C>G;1250A>G]	NP_001276792.1:p.[Pro415Ala;His417Arg]
NM_001289864.1:c.[286C>G;293A>G]	NP_001276793.1:p.[Pro96Ala;His98Arg]
NM_016831.2:c.[1240C>G;1247A>G]	NP_058515.1:p.[Pro414Ala;His416Arg]
XM_005263521.2:c.[1243C>G;1250A>G]	XP_005263578.1:p.[Pro415Ala;His417Arg]
XM_005263522.2:c.[1240C>G;1247A>G]	XP_005263579.1:p.[Pro414Ala;His416Arg]
XM_005263523.2:c.[1243C>G;1250A>G]	XP_005263580.1:p.[Pro415Ala;His417Arg]
XM_005263524.2:c.[1243C>G;1250A>G]	XP_005263581.1:p.[Pro415Ala;His417Arg]
XM_005263529.2:c.[718C>G;725A>G]	XP_005263586.1:p.[Pro240Ala;His242Arg]
XM_011542384.1:c.[1243C>G;1250A>G]	XP_011540686.1:p.[Pro415Ala;His417Arg]
XM_011542385.1:c.[1243C>G;1250A>G]	XP_011540687.1:p.[Pro415Ala;His417Arg]
XM_011542386.1:c.[1243C>G;1250A>G]	XP_011540688.1:p.[Pro415Ala;His417Arg]
XM_011542387.1:c.[1075C>G;1082A>G]	XP_011540689.1:p.[Pro359Ala;His361Arg]
XM_011542388.1:c.[895C>G;902A>G]	XP_011540690.1:p.[Pro299Ala;His301Arg]
XM_011542389.1:c.[880C>G;887A>G]	XP_011540691.1:p.[Pro294Ala;His296Arg]
XM_011542390.1:c.[1243C>G;1250A>G]	XP_011540692.1:p.[Pro415Ala;His417Arg]
XM_005263524.4:c.[1243C>G;1250A>G]	XP_005263581.1:p.[Pro415Ala;His417Arg]
XM_017002723.2:c.[1240C>G;1247A>G]	XP_016858212.1:p.[Pro414Ala;His416Arg]
XM_017002724.2:c.[1240C>G;1247A>G]	XP_016858213.1:p.[Pro414Ala;His416Arg]
XM_017002726.2:c.[1240C>G;1247A>G]	XP_016858215.1:p.[Pro414Ala;His416Arg]
XM_017002727.1:c.[1075C>G;1082A>G]	XP_016858216.1:p.[Pro359Ala;His361Arg]
XM_017002728.1:c.[895C>G;902A>G]	XP_016858217.1:p.[Pro299Ala;His301Arg]
XM_017002729.1:c.[880C>G;887A>G]	XP_016858218.1:p.[Pro294Ala;His296Arg]
XM_017002730.2:c.[895C>G;902A>G]	XP_016858219.1:p.[Pro299Ala;His301Arg]
XM_017002731.2:c.[895C>G;902A>G]	XP_016858220.1:p.[Pro299Ala;His301Arg]
XM_017002732.1:c.[895C>G;902A>G]	XP_016858221.1:p.[Pro299Ala;His301Arg]
XM_017002733.2:c.[718C>G;725A>G]	XP_016858222.1:p.[Pro240Ala;His242Arg]
XM_017002734.1:c.[718C>G;725A>G]	XP_016858223.1:p.[Pro240Ala;His242Arg]
XM_017002735.2:c.[718C>G;725A>G]	XP_016858224.1:p.[Pro240Ala;His242Arg]
XM_017002737.1:c.[-129C>G;-122A>G]	XP_016858226.1:n.[-129C>G;-122A>G]
XM_017002738.2:c.[-129C>G;-122A>G]	XP_016858227.1:n.[-129C>G;-122A>G]
XM_024450585.1:c.[1243C>G;1250A>G]	XP_024306353.1:p.[Pro415Ala;His417Arg]
XM_024450586.1:c.[1243C>G;1250A>G]	XP_024306354.1:p.[Pro415Ala;His417Arg]
XM_024450587.1:c.[1243C>G;1250A>G]	XP_024306355.1:p.[Pro415Ala;His417Arg]
XM_024450588.1:c.[1243C>G;1250A>G]	XP_024306356.1:p.[Pro415Ala;His417Arg]
XM_024450590.1:c.[1240C>G;1247A>G]	XP_024306358.1:p.[Pro414Ala;His416Arg]
XM_024450611.1:c.[718C>G;725A>G]	XP_024306379.1:p.[Pro240Ala;His242Arg]
XM_024450612.1:c.[718C>G;725A>G]	XP_024306380.1:p.[Pro240Ala;His242Arg]
NM_001289861.2:c.[1243C>G;1250A>G]	NP_001276790.1:p.[Pro415Ala;His417Arg]
NM_001289862.2:c.[1243C>G;1250A>G]	NP_001276791.1:p.[Pro415Ala;His417Arg]
NM_001289863.3:c.[1243C>G;1250A>G]	NP_001276792.1:p.[Pro415Ala;His417Arg]
NM_001289864.3:c.[286C>G;293A>G]	NP_001276793.1:p.[Pro96Ala;His98Arg]
NM_001377275.1:c.[1243C>G;1250A>G] MANE Select	NP_001364204.1:p.[Pro415Ala;His417Arg]
NM_001377276.1:c.[1243C>G;1250A>G]	NP_001364205.1:p.[Pro415Ala;His417Arg]
NM_016831.4:c.[1240C>G;1247A>G]	NP_058515.1:p.[Pro414Ala;His416Arg]