Canonical Allele Identifier: CA1953974152
Gene: CYP2R1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14879122A= , CM000673.2:g.14879122A= GRCh38
NC_000011.9:g.14900668A= , CM000673.1:g.14900668A= GRCh37
NC_000011.8:g.14857244A= NCBI36
NG_007936.1:g.18084T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334636.10:c.1322T= MANE Select ENSP00000334592.5:p.Phe441=
ENST00000334636.9:c.1322T= ENSP00000334592.5:p.Phe441=
ENST00000525015.1:c.152T=
ENST00000530609.5:c.*918T= ENSP00000466060.1:n.*918T=
ENST00000532378.5:c.623T= ENSP00000435484.1:p.Phe208=
ENST00000532805.1:c.*430T= ENSP00000465097.1:n.*430T=
ENST00000534686.5:c.*682T= ENSP00000432087.2:n.*682T=
NM_024514.4:c.1322T= NP_078790.2:p.Phe441=
XM_005252788.1:c.1178T= XP_005252845.1:p.Phe393=
XM_005252789.2:c.1160T= XP_005252846.1:p.Phe387=
XM_005252791.3:c.977T= XP_005252848.1:p.Phe326=
XM_006718142.2:c.1277T= XP_006718205.1:p.Phe426=
XM_011519894.1:c.977T= XP_011518196.1:p.Phe326=
XM_011519895.1:c.977T= XP_011518197.1:p.Phe326=
XM_011519896.1:c.977T= XP_011518198.1:p.Phe326=
XM_011519897.1:c.977T= XP_011518199.1:p.Phe326=
XM_011519898.1:c.977T= XP_011518200.1:p.Phe326=
XR_242777.2:n.1139T=
XM_005252788.2:c.1178T= XP_005252845.1:p.Phe393=
XM_005252789.3:c.1160T= XP_005252846.1:p.Phe387=
XM_011519895.2:c.977T= XP_011518197.1:p.Phe326=
XM_011519898.3:c.977T= XP_011518200.1:p.Phe326=
XM_017017190.2:c.1157T= XP_016872679.1:p.Phe386=
XM_017017191.2:c.977T= XP_016872680.1:p.Phe326=
XM_017017192.2:c.977T= XP_016872681.1:p.Phe326=
XM_017017193.2:c.977T= XP_016872682.1:p.Phe326=
XM_017017194.2:c.977T= XP_016872683.1:p.Phe326=
XM_024448345.1:c.1157T= XP_024304113.1:p.Phe386=
XM_024448346.1:c.977T= XP_024304114.1:p.Phe326=
XM_024448347.1:c.977T= XP_024304115.1:p.Phe326=
XM_024448348.1:c.977T= XP_024304116.1:p.Phe326=
XR_002957123.1:n.1102T=
XR_002957124.1:n.1368T=
XR_242777.3:n.1139T=
NM_001377214.1:c.977T= NP_001364143.1:p.Phe326=
NM_001377215.1:c.977T= NP_001364144.1:p.Phe326=
NM_001377216.1:c.977T= NP_001364145.1:p.Phe326=
NM_001377217.1:c.1160T= NP_001364146.1:p.Phe387=
NM_001377227.1:c.977T= NP_001364156.1:p.Phe326=
NM_024514.5:c.1322T= MANE Select NP_078790.2:p.Phe441=
NM_001400558.1:c.977T= NP_001387487.1:p.Phe326=
NM_001400559.1:c.977T= NP_001387488.1:p.Phe326=
NM_001400560.1:c.977T= NP_001387489.1:p.Phe326=
NM_001400561.1:c.977T= NP_001387490.1:p.Phe326=
NM_001400562.1:c.623T= NP_001387491.1:p.Phe208=
NM_001400563.1:c.623T= NP_001387492.1:p.Phe208=
NM_001400564.1:c.623T= NP_001387493.1:p.Phe208=
NM_001400565.1:c.623T= NP_001387494.1:p.Phe208=
NM_001400566.1:c.344T= NP_001387495.1:p.Phe115=
NM_001400567.1:c.1178T= NP_001387496.1:p.Phe393=
NM_001400568.1:c.1277T= NP_001387497.1:p.Phe426=
NR_174512.1:n.1189T=
NR_174513.1:n.1038T=
NR_174514.1:n.1413T=
NR_174515.1:n.1822T=
NR_174516.1:n.1000T=
NR_174517.1:n.536T=
NR_174518.1:n.1633T=
NR_174519.1:n.1380T=
NR_174520.1:n.1171T=
NR_174521.1:n.1671T=
NR_174522.1:n.1169T=
NR_174523.1:n.1580T=