Canonical Allele Identifier: CA1953974162
Gene: CYP2R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14879147C= , CM000673.2:g.14879147C= GRCh38
NC_000011.9:g.14900693C= , CM000673.1:g.14900693C= GRCh37
NC_000011.8:g.14857269C= NCBI36
NG_007936.1:g.18059G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334636.10:c.1297G= MANE Select ENSP00000334592.5:p.Ala433=
ENST00000334636.9:c.1297G= ENSP00000334592.5:p.Ala433=
ENST00000525015.1:c.127G=
ENST00000530609.5:c.*893G= ENSP00000466060.1:n.*893G=
ENST00000532378.5:c.598G= ENSP00000435484.1:p.Ala200=
ENST00000532805.1:c.*405G= ENSP00000465097.1:n.*405G=
ENST00000534686.5:c.*657G= ENSP00000432087.2:n.*657G=
NM_024514.4:c.1297G= NP_078790.2:p.Ala433=
XM_005252788.1:c.1153G= XP_005252845.1:p.Ala385=
XM_005252789.2:c.1135G= XP_005252846.1:p.Ala379=
XM_005252791.3:c.952G= XP_005252848.1:p.Ala318=
XM_006718142.2:c.1252G= XP_006718205.1:p.Ala418=
XM_011519894.1:c.952G= XP_011518196.1:p.Ala318=
XM_011519895.1:c.952G= XP_011518197.1:p.Ala318=
XM_011519896.1:c.952G= XP_011518198.1:p.Ala318=
XM_011519897.1:c.952G= XP_011518199.1:p.Ala318=
XM_011519898.1:c.952G= XP_011518200.1:p.Ala318=
XR_242777.2:n.1114G=
XM_005252788.2:c.1153G= XP_005252845.1:p.Ala385=
XM_005252789.3:c.1135G= XP_005252846.1:p.Ala379=
XM_011519895.2:c.952G= XP_011518197.1:p.Ala318=
XM_011519898.3:c.952G= XP_011518200.1:p.Ala318=
XM_017017190.2:c.1132G= XP_016872679.1:p.Ala378=
XM_017017191.2:c.952G= XP_016872680.1:p.Ala318=
XM_017017192.2:c.952G= XP_016872681.1:p.Ala318=
XM_017017193.2:c.952G= XP_016872682.1:p.Ala318=
XM_017017194.2:c.952G= XP_016872683.1:p.Ala318=
XM_024448345.1:c.1132G= XP_024304113.1:p.Ala378=
XM_024448346.1:c.952G= XP_024304114.1:p.Ala318=
XM_024448347.1:c.952G= XP_024304115.1:p.Ala318=
XM_024448348.1:c.952G= XP_024304116.1:p.Ala318=
XR_002957123.1:n.1077G=
XR_002957124.1:n.1343G=
XR_242777.3:n.1114G=
NM_001377214.1:c.952G= NP_001364143.1:p.Ala318=
NM_001377215.1:c.952G= NP_001364144.1:p.Ala318=
NM_001377216.1:c.952G= NP_001364145.1:p.Ala318=
NM_001377217.1:c.1135G= NP_001364146.1:p.Ala379=
NM_001377227.1:c.952G= NP_001364156.1:p.Ala318=
NM_024514.5:c.1297G= MANE Select NP_078790.2:p.Ala433=
NM_001400558.1:c.952G= NP_001387487.1:p.Ala318=
NM_001400559.1:c.952G= NP_001387488.1:p.Ala318=
NM_001400560.1:c.952G= NP_001387489.1:p.Ala318=
NM_001400561.1:c.952G= NP_001387490.1:p.Ala318=
NM_001400562.1:c.598G= NP_001387491.1:p.Ala200=
NM_001400563.1:c.598G= NP_001387492.1:p.Ala200=
NM_001400564.1:c.598G= NP_001387493.1:p.Ala200=
NM_001400565.1:c.598G= NP_001387494.1:p.Ala200=
NM_001400566.1:c.319G= NP_001387495.1:p.Ala107=
NM_001400567.1:c.1153G= NP_001387496.1:p.Ala385=
NM_001400568.1:c.1252G= NP_001387497.1:p.Ala418=
NR_174512.1:n.1164G=
NR_174513.1:n.1013G=
NR_174514.1:n.1388G=
NR_174515.1:n.1797G=
NR_174516.1:n.975G=
NR_174517.1:n.511G=
NR_174518.1:n.1608G=
NR_174519.1:n.1355G=
NR_174520.1:n.1146G=
NR_174521.1:n.1646G=
NR_174522.1:n.1144G=
NR_174523.1:n.1555G=