Canonical Allele Identifier: CA338134752

Gene: PER3

Linked Data

• gnomAD v4: 1-7803704-C-T
• MyVariant Identifiers: chr1:g.7863764C>T (hg19) ; chr1:g.7803704C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7803704C>T , CM000663.2:g.7803704C>T	GRCh38
NC_000001.10:g.7863764C>T , CM000663.1:g.7863764C>T	GRCh37
NC_000001.9:g.7786351C>T	NCBI36
NG_046850.1:g.24325C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377532.8:c.992C>T MANE Select	ENSP00000366755.3:p.Ala331Val
ENST00000361923.2:c.989C>T	ENSP00000355031.2:p.Ala330Val
ENST00000377532.7:c.992C>T	ENSP00000366755.3:p.Ala331Val
ENST00000377541.5:c.989C>T	ENSP00000366764.1:p.Ala330Val
ENST00000463106.1:n.116C>T
ENST00000613533.4:c.992C>T	ENSP00000482093.1:p.Ala331Val
ENST00000614998.4:c.992C>T	ENSP00000479223.1:p.Ala331Val
NM_001289861.1:c.992C>T	NP_001276790.1:p.Ala331Val
NM_001289862.1:c.992C>T	NP_001276791.1:p.Ala331Val
NM_001289863.1:c.992C>T	NP_001276792.1:p.Ala331Val
NM_001289864.1:c.35C>T	NP_001276793.1:p.Ala12Val
NM_016831.2:c.989C>T	NP_058515.1:p.Ala330Val
XM_005263521.2:c.992C>T	XP_005263578.1:p.Ala331Val
XM_005263522.2:c.989C>T	XP_005263579.1:p.Ala330Val
XM_005263523.2:c.992C>T	XP_005263580.1:p.Ala331Val
XM_005263524.2:c.992C>T	XP_005263581.1:p.Ala331Val
XM_005263529.2:c.467C>T	XP_005263586.1:p.Ala156Val
XM_011542384.1:c.992C>T	XP_011540686.1:p.Ala331Val
XM_011542385.1:c.992C>T	XP_011540687.1:p.Ala331Val
XM_011542386.1:c.992C>T	XP_011540688.1:p.Ala331Val
XM_011542387.1:c.824C>T	XP_011540689.1:p.Ala275Val
XM_011542388.1:c.644C>T	XP_011540690.1:p.Ala215Val
XM_011542389.1:c.629C>T	XP_011540691.1:p.Ala210Val
XM_011542390.1:c.992C>T	XP_011540692.1:p.Ala331Val
XM_005263524.4:c.992C>T	XP_005263581.1:p.Ala331Val
XM_017002723.2:c.989C>T	XP_016858212.1:p.Ala330Val
XM_017002724.2:c.989C>T	XP_016858213.1:p.Ala330Val
XM_017002726.2:c.989C>T	XP_016858215.1:p.Ala330Val
XM_017002727.1:c.824C>T	XP_016858216.1:p.Ala275Val
XM_017002728.1:c.644C>T	XP_016858217.1:p.Ala215Val
XM_017002729.1:c.629C>T	XP_016858218.1:p.Ala210Val
XM_017002730.2:c.644C>T	XP_016858219.1:p.Ala215Val
XM_017002731.2:c.644C>T	XP_016858220.1:p.Ala215Val
XM_017002732.1:c.644C>T	XP_016858221.1:p.Ala215Val
XM_017002733.2:c.467C>T	XP_016858222.1:p.Ala156Val
XM_017002734.1:c.467C>T	XP_016858223.1:p.Ala156Val
XM_017002735.2:c.467C>T	XP_016858224.1:p.Ala156Val
XM_017002737.1:c.-274C>T	XP_016858226.1:n.-274C>T
XM_017002738.2:c.-274C>T	XP_016858227.1:n.-274C>T
XM_024450585.1:c.992C>T	XP_024306353.1:p.Ala331Val
XM_024450586.1:c.992C>T	XP_024306354.1:p.Ala331Val
XM_024450587.1:c.992C>T	XP_024306355.1:p.Ala331Val
XM_024450588.1:c.992C>T	XP_024306356.1:p.Ala331Val
XM_024450590.1:c.989C>T	XP_024306358.1:p.Ala330Val
XM_024450611.1:c.467C>T	XP_024306379.1:p.Ala156Val
XM_024450612.1:c.467C>T	XP_024306380.1:p.Ala156Val
NM_001289861.2:c.992C>T	NP_001276790.1:p.Ala331Val
NM_001289862.2:c.992C>T	NP_001276791.1:p.Ala331Val
NM_001289863.3:c.992C>T	NP_001276792.1:p.Ala331Val
NM_001289864.3:c.35C>T	NP_001276793.1:p.Ala12Val
NM_001377275.1:c.992C>T MANE Select	NP_001364204.1:p.Ala331Val
NM_001377276.1:c.992C>T	NP_001364205.1:p.Ala331Val
NM_016831.4:c.989C>T	NP_058515.1:p.Ala330Val