Canonical Allele Identifier: CA379744662

Gene: CYP2R1

Linked Data

• MyVariant Identifiers: chr11:g.14900669A>C (hg19) ; chr11:g.14879123A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879123A>C , CM000673.2:g.14879123A>C	GRCh38
NC_000011.9:g.14900669A>C , CM000673.1:g.14900669A>C	GRCh37
NC_000011.8:g.14857245A>C	NCBI36
NG_007936.1:g.18083T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334636.10:c.1321T>G MANE Select	ENSP00000334592.5:p.Phe441Val
ENST00000334636.9:c.1321T>G	ENSP00000334592.5:p.Phe441Val
ENST00000525015.1:c.151T>G
ENST00000530609.5:c.*917T>G	ENSP00000466060.1:n.*917T>G
ENST00000532378.5:c.622T>G	ENSP00000435484.1:p.Phe208Val
ENST00000532805.1:c.*429T>G	ENSP00000465097.1:n.*429T>G
ENST00000534686.5:c.*681T>G	ENSP00000432087.2:n.*681T>G
NM_024514.4:c.1321T>G	NP_078790.2:p.Phe441Val
XM_005252788.1:c.1177T>G	XP_005252845.1:p.Phe393Val
XM_005252789.2:c.1159T>G	XP_005252846.1:p.Phe387Val
XM_005252791.3:c.976T>G	XP_005252848.1:p.Phe326Val
XM_006718142.2:c.1276T>G	XP_006718205.1:p.Phe426Val
XM_011519894.1:c.976T>G	XP_011518196.1:p.Phe326Val
XM_011519895.1:c.976T>G	XP_011518197.1:p.Phe326Val
XM_011519896.1:c.976T>G	XP_011518198.1:p.Phe326Val
XM_011519897.1:c.976T>G	XP_011518199.1:p.Phe326Val
XM_011519898.1:c.976T>G	XP_011518200.1:p.Phe326Val
XR_242777.2:n.1138T>G
XM_005252788.2:c.1177T>G	XP_005252845.1:p.Phe393Val
XM_005252789.3:c.1159T>G	XP_005252846.1:p.Phe387Val
XM_011519895.2:c.976T>G	XP_011518197.1:p.Phe326Val
XM_011519898.3:c.976T>G	XP_011518200.1:p.Phe326Val
XM_017017190.2:c.1156T>G	XP_016872679.1:p.Phe386Val
XM_017017191.2:c.976T>G	XP_016872680.1:p.Phe326Val
XM_017017192.2:c.976T>G	XP_016872681.1:p.Phe326Val
XM_017017193.2:c.976T>G	XP_016872682.1:p.Phe326Val
XM_017017194.2:c.976T>G	XP_016872683.1:p.Phe326Val
XM_024448345.1:c.1156T>G	XP_024304113.1:p.Phe386Val
XM_024448346.1:c.976T>G	XP_024304114.1:p.Phe326Val
XM_024448347.1:c.976T>G	XP_024304115.1:p.Phe326Val
XM_024448348.1:c.976T>G	XP_024304116.1:p.Phe326Val
XR_002957123.1:n.1101T>G
XR_002957124.1:n.1367T>G
XR_242777.3:n.1138T>G
NM_001377214.1:c.976T>G	NP_001364143.1:p.Phe326Val
NM_001377215.1:c.976T>G	NP_001364144.1:p.Phe326Val
NM_001377216.1:c.976T>G	NP_001364145.1:p.Phe326Val
NM_001377217.1:c.1159T>G	NP_001364146.1:p.Phe387Val
NM_001377227.1:c.976T>G	NP_001364156.1:p.Phe326Val
NM_024514.5:c.1321T>G MANE Select	NP_078790.2:p.Phe441Val
NM_001400558.1:c.976T>G	NP_001387487.1:p.Phe326Val
NM_001400559.1:c.976T>G	NP_001387488.1:p.Phe326Val
NM_001400560.1:c.976T>G	NP_001387489.1:p.Phe326Val
NM_001400561.1:c.976T>G	NP_001387490.1:p.Phe326Val
NM_001400562.1:c.622T>G	NP_001387491.1:p.Phe208Val
NM_001400563.1:c.622T>G	NP_001387492.1:p.Phe208Val
NM_001400564.1:c.622T>G	NP_001387493.1:p.Phe208Val
NM_001400565.1:c.622T>G	NP_001387494.1:p.Phe208Val
NM_001400566.1:c.343T>G	NP_001387495.1:p.Phe115Val
NM_001400567.1:c.1177T>G	NP_001387496.1:p.Phe393Val
NM_001400568.1:c.1276T>G	NP_001387497.1:p.Phe426Val
NR_174512.1:n.1188T>G
NR_174513.1:n.1037T>G
NR_174514.1:n.1412T>G
NR_174515.1:n.1821T>G
NR_174516.1:n.999T>G
NR_174517.1:n.535T>G
NR_174518.1:n.1632T>G
NR_174519.1:n.1379T>G
NR_174520.1:n.1170T>G
NR_174521.1:n.1670T>G
NR_174522.1:n.1168T>G
NR_174523.1:n.1579T>G