Canonical Allele Identifier: CA379733408

Gene: CYP2R1

Linked Data

• MyVariant Identifiers: chr11:g.14907378T>A (hg19) ; chr11:g.14885832T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14885832T>A , CM000673.2:g.14885832T>A	GRCh38
NC_000011.9:g.14907378T>A , CM000673.1:g.14907378T>A	GRCh37
NC_000011.8:g.14863954T>A	NCBI36
NG_007936.1:g.11374A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334636.10:c.311A>T MANE Select	ENSP00000334592.5:p.Glu104Val
ENST00000334636.9:c.311A>T	ENSP00000334592.5:p.Glu104Val
ENST00000525015.1:c.10A>T
ENST00000526276.5:n.215A>T
ENST00000526489.5:n.186A>T
ENST00000529043.1:n.291A>T
ENST00000530609.5:c.21A>T	ENSP00000466060.1:p.Arg7=
ENST00000532378.5:c.21A>T	ENSP00000435484.1:p.Arg7=
ENST00000532641.1:n.146A>T
ENST00000532805.1:c.21A>T	ENSP00000465097.1:p.Arg7=
ENST00000534686.5:c.21A>T	ENSP00000432087.2:p.Arg7=
NM_024514.4:c.311A>T	NP_078790.2:p.Glu104Val
XM_005252788.1:c.167A>T	XP_005252845.1:p.Glu56Val
XM_005252789.2:c.149A>T	XP_005252846.1:p.Glu50Val
XM_005252791.3:c.-35A>T	XP_005252848.1:n.-35A>T
XM_006718142.2:c.266A>T	XP_006718205.1:p.Glu89Val
XM_011519894.1:c.-35A>T	XP_011518196.1:n.-35A>T
XM_011519895.1:c.-35A>T	XP_011518197.1:n.-35A>T
XM_011519896.1:c.-35A>T	XP_011518198.1:n.-35A>T
XM_011519897.1:c.-35A>T	XP_011518199.1:n.-35A>T
XM_011519898.1:c.-35A>T	XP_011518200.1:n.-35A>T
XR_242777.2:n.364A>T
XM_005252788.2:c.167A>T	XP_005252845.1:p.Glu56Val
XM_005252789.3:c.149A>T	XP_005252846.1:p.Glu50Val
XM_011519895.2:c.-35A>T	XP_011518197.1:n.-35A>T
XM_011519898.3:c.-35A>T	XP_011518200.1:n.-35A>T
XM_017017190.2:c.146A>T	XP_016872679.1:p.Glu49Val
XM_017017191.2:c.-35A>T	XP_016872680.1:n.-35A>T
XM_017017192.2:c.-35A>T	XP_016872681.1:n.-35A>T
XM_017017193.2:c.-35A>T	XP_016872682.1:n.-35A>T
XM_017017194.2:c.-35A>T	XP_016872683.1:n.-35A>T
XM_024448345.1:c.146A>T	XP_024304113.1:p.Glu49Val
XM_024448346.1:c.-35A>T	XP_024304114.1:n.-35A>T
XM_024448347.1:c.-35A>T	XP_024304115.1:n.-35A>T
XM_024448348.1:c.-35A>T	XP_024304116.1:n.-35A>T
XR_002957123.1:n.327A>T
XR_002957124.1:n.593A>T
XR_242777.3:n.364A>T
NM_001377214.1:c.-35A>T	NP_001364143.1:n.-35A>T
NM_001377215.1:c.-35A>T	NP_001364144.1:n.-35A>T
NM_001377216.1:c.-35A>T	NP_001364145.1:n.-35A>T
NM_001377217.1:c.149A>T	NP_001364146.1:p.Glu50Val
NM_001377227.1:c.-35A>T	NP_001364156.1:n.-35A>T
NM_024514.5:c.311A>T MANE Select	NP_078790.2:p.Glu104Val
NM_001400558.1:c.-35A>T	NP_001387487.1:n.-35A>T
NM_001400559.1:c.-35A>T	NP_001387488.1:n.-35A>T
NM_001400560.1:c.-35A>T	NP_001387489.1:n.-35A>T
NM_001400561.1:c.-35A>T	NP_001387490.1:n.-35A>T
NM_001400562.1:c.21A>T	NP_001387491.1:p.Arg7=
NM_001400563.1:c.21A>T	NP_001387492.1:p.Arg7=
NM_001400564.1:c.21A>T	NP_001387493.1:p.Arg7=
NM_001400565.1:c.21A>T	NP_001387494.1:p.Arg7=
NM_001400566.1:c.-35A>T	NP_001387495.1:n.-35A>T
NM_001400567.1:c.167A>T	NP_001387496.1:p.Glu56Val
NM_001400568.1:c.266A>T	NP_001387497.1:p.Glu89Val
NR_174512.1:n.1047A>T
NR_174513.1:n.896A>T
NR_174514.1:n.1047A>T
NR_174515.1:n.1047A>T
NR_174516.1:n.858A>T
NR_174517.1:n.394A>T
NR_174518.1:n.858A>T
NR_174519.1:n.605A>T
NR_174520.1:n.805A>T
NR_174521.1:n.896A>T
NR_174522.1:n.394A>T
NR_174523.1:n.805A>T