Canonical Allele Identifier: CA653970047
Gene: CYP2R1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14879501del , CM000673.2:g.14879501del GRCh38
NC_000011.9:g.14901047del , CM000673.1:g.14901047del GRCh37
NC_000011.8:g.14857623del NCBI36
NG_007936.1:g.17705del

Transcript Alleles

HGVS Amino-acid Change
ENST00000334636.10:c.1001-58del MANE Select ENSP00000334592.5:n.1001-58del
ENST00000334636.9:c.1001-58del ENSP00000334592.5:n.1001-58del
ENST00000525015.1:c.67-294del
ENST00000530609.5:c.*597-58del ENSP00000466060.1:n.*597-58del
ENST00000532378.5:c.302-58del ENSP00000435484.1:n.302-58del
ENST00000532805.1:c.*353-302del ENSP00000465097.1:n.*353-302del
ENST00000534686.5:c.*597-294del ENSP00000432087.2:n.*597-294del
NM_024514.4:c.1001-58del NP_078790.2:n.1001-58del
XM_005252788.1:c.857-58del XP_005252845.1:n.857-58del
XM_005252789.2:c.839-58del XP_005252846.1:n.839-58del
XM_005252791.3:c.656-58del XP_005252848.1:n.656-58del
XM_006718142.2:c.956-58del XP_006718205.1:n.956-58del
XM_011519894.1:c.656-58del XP_011518196.1:n.656-58del
XM_011519895.1:c.656-58del XP_011518197.1:n.656-58del
XM_011519896.1:c.656-58del XP_011518198.1:n.656-58del
XM_011519897.1:c.656-58del XP_011518199.1:n.656-58del
XM_011519898.1:c.656-58del XP_011518200.1:n.656-58del
XR_242777.2:n.1054-294del
XM_005252788.2:c.857-58del XP_005252845.1:n.857-58del
XM_005252789.3:c.839-58del XP_005252846.1:n.839-58del
XM_011519895.2:c.656-58del XP_011518197.1:n.656-58del
XM_011519898.3:c.656-58del XP_011518200.1:n.656-58del
XM_017017190.2:c.836-58del XP_016872679.1:n.836-58del
XM_017017191.2:c.656-58del XP_016872680.1:n.656-58del
XM_017017192.2:c.656-58del XP_016872681.1:n.656-58del
XM_017017193.2:c.656-58del XP_016872682.1:n.656-58del
XM_017017194.2:c.656-58del XP_016872683.1:n.656-58del
XM_024448345.1:c.836-58del XP_024304113.1:n.836-58del
XM_024448346.1:c.656-58del XP_024304114.1:n.656-58del
XM_024448347.1:c.656-58del XP_024304115.1:n.656-58del
XM_024448348.1:c.656-58del XP_024304116.1:n.656-58del
XR_002957123.1:n.1017-294del
XR_002957124.1:n.1283-294del
XR_242777.3:n.1054-294del
NM_001377214.1:c.656-58del NP_001364143.1:n.656-58del
NM_001377215.1:c.656-58del NP_001364144.1:n.656-58del
NM_001377216.1:c.656-58del NP_001364145.1:n.656-58del
NM_001377217.1:c.839-58del NP_001364146.1:n.839-58del
NM_001377227.1:c.656-58del NP_001364156.1:n.656-58del
NM_024514.5:c.1001-58del MANE Select NP_078790.2:n.1001-58del
NM_001400558.1:c.656-58del NP_001387487.1:n.656-58del
NM_001400559.1:c.656-58del NP_001387488.1:n.656-58del
NM_001400560.1:c.656-58del NP_001387489.1:n.656-58del
NM_001400561.1:c.656-58del NP_001387490.1:n.656-58del
NM_001400562.1:c.302-58del NP_001387491.1:n.302-58del
NM_001400563.1:c.302-58del NP_001387492.1:n.302-58del
NM_001400564.1:c.302-58del NP_001387493.1:n.302-58del
NM_001400565.1:c.302-58del NP_001387494.1:n.302-58del
NM_001400566.1:c.23-58del NP_001387495.1:n.23-58del
NM_001400567.1:c.857-58del NP_001387496.1:n.857-58del
NM_001400568.1:c.956-58del NP_001387497.1:n.956-58del
NR_174512.1:n.1104-294del
NR_174513.1:n.953-294del
NR_174514.1:n.1328-294del
NR_174515.1:n.1737-294del
NR_174516.1:n.915-294del
NR_174517.1:n.451-294del
NR_174518.1:n.1548-294del
NR_174519.1:n.1295-294del
NR_174520.1:n.1086-294del
NR_174521.1:n.1586-294del
NR_174522.1:n.1084-294del
NR_174523.1:n.1495-294del