Canonical Allele Identifier: CA1953974245

Gene: CYP2R1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879386_14879387delinsTC , CM000673.2:g.14879386_14879387delinsTC	GRCh38
NC_000011.9:g.14900932_14900933delinsTC , CM000673.1:g.14900932_14900933delinsTC	GRCh37
NC_000011.8:g.14857508_14857509delinsTC	NCBI36
NG_007936.1:g.17819_17820delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000334636.10:c.1057_1058delinsGA MANE Select	ENSP00000334592.5:p.Asp353=
ENST00000334636.9:c.1057_1058delinsGA	ENSP00000334592.5:p.Asp353=
ENST00000525015.1:c.67-180_67-179delinsGA
ENST00000530609.5:c.*653_*654delinsGA	ENSP00000466060.1:n.*653_*654delinsGA
ENST00000532378.5:c.358_359delinsGA	ENSP00000435484.1:p.Asp120=
ENST00000532805.1:c.*353-188_*353-187delinsGA	ENSP00000465097.1:n.*353-188_*353-187deli...
ENST00000534686.5:c.*597-180_*597-179delinsGA	ENSP00000432087.2:n.*597-180_*597-179deli...
NM_024514.4:c.1057_1058delinsGA	NP_078790.2:p.Asp353=
XM_005252788.1:c.913_914delinsGA	XP_005252845.1:p.Asp305=
XM_005252789.2:c.895_896delinsGA	XP_005252846.1:p.Asp299=
XM_005252791.3:c.712_713delinsGA	XP_005252848.1:p.Asp238=
XM_006718142.2:c.1012_1013delinsGA	XP_006718205.1:p.Asp338=
XM_011519894.1:c.712_713delinsGA	XP_011518196.1:p.Asp238=
XM_011519895.1:c.712_713delinsGA	XP_011518197.1:p.Asp238=
XM_011519896.1:c.712_713delinsGA	XP_011518198.1:p.Asp238=
XM_011519897.1:c.712_713delinsGA	XP_011518199.1:p.Asp238=
XM_011519898.1:c.712_713delinsGA	XP_011518200.1:p.Asp238=
XR_242777.2:n.1054-180_1054-179delinsGA
XM_005252788.2:c.913_914delinsGA	XP_005252845.1:p.Asp305=
XM_005252789.3:c.895_896delinsGA	XP_005252846.1:p.Asp299=
XM_011519895.2:c.712_713delinsGA	XP_011518197.1:p.Asp238=
XM_011519898.3:c.712_713delinsGA	XP_011518200.1:p.Asp238=
XM_017017190.2:c.892_893delinsGA	XP_016872679.1:p.Asp298=
XM_017017191.2:c.712_713delinsGA	XP_016872680.1:p.Asp238=
XM_017017192.2:c.712_713delinsGA	XP_016872681.1:p.Asp238=
XM_017017193.2:c.712_713delinsGA	XP_016872682.1:p.Asp238=
XM_017017194.2:c.712_713delinsGA	XP_016872683.1:p.Asp238=
XM_024448345.1:c.892_893delinsGA	XP_024304113.1:p.Asp298=
XM_024448346.1:c.712_713delinsGA	XP_024304114.1:p.Asp238=
XM_024448347.1:c.712_713delinsGA	XP_024304115.1:p.Asp238=
XM_024448348.1:c.712_713delinsGA	XP_024304116.1:p.Asp238=
XR_002957123.1:n.1017-180_1017-179delinsGA
XR_002957124.1:n.1283-180_1283-179delinsGA
XR_242777.3:n.1054-180_1054-179delinsGA
NM_001377214.1:c.712_713delinsGA	NP_001364143.1:p.Asp238=
NM_001377215.1:c.712_713delinsGA	NP_001364144.1:p.Asp238=
NM_001377216.1:c.712_713delinsGA	NP_001364145.1:p.Asp238=
NM_001377217.1:c.895_896delinsGA	NP_001364146.1:p.Asp299=
NM_001377227.1:c.712_713delinsGA	NP_001364156.1:p.Asp238=
NM_024514.5:c.1057_1058delinsGA MANE Select	NP_078790.2:p.Asp353=
NM_001400558.1:c.712_713delinsGA	NP_001387487.1:p.Asp238=
NM_001400559.1:c.712_713delinsGA	NP_001387488.1:p.Asp238=
NM_001400560.1:c.712_713delinsGA	NP_001387489.1:p.Asp238=
NM_001400561.1:c.712_713delinsGA	NP_001387490.1:p.Asp238=
NM_001400562.1:c.358_359delinsGA	NP_001387491.1:p.Asp120=
NM_001400563.1:c.358_359delinsGA	NP_001387492.1:p.Asp120=
NM_001400564.1:c.358_359delinsGA	NP_001387493.1:p.Asp120=
NM_001400565.1:c.358_359delinsGA	NP_001387494.1:p.Asp120=
NM_001400566.1:c.79_80delinsGA	NP_001387495.1:p.Asp27=
NM_001400567.1:c.913_914delinsGA	NP_001387496.1:p.Asp305=
NM_001400568.1:c.1012_1013delinsGA	NP_001387497.1:p.Asp338=
NR_174512.1:n.1104-180_1104-179delinsGA
NR_174513.1:n.953-180_953-179delinsGA
NR_174514.1:n.1328-180_1328-179delinsGA
NR_174515.1:n.1737-180_1737-179delinsGA
NR_174516.1:n.915-180_915-179delinsGA
NR_174517.1:n.451-180_451-179delinsGA
NR_174518.1:n.1548-180_1548-179delinsGA
NR_174519.1:n.1295-180_1295-179delinsGA
NR_174520.1:n.1086-180_1086-179delinsGA
NR_174521.1:n.1586-180_1586-179delinsGA
NR_174522.1:n.1084-180_1084-179delinsGA
NR_174523.1:n.1495-180_1495-179delinsGA