Canonical Allele Identifier: CA379744653

Gene: CYP2R1

Linked Data

• MyVariant Identifiers: chr11:g.14900665G>T (hg19) ; chr11:g.14879119G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879119G>T , CM000673.2:g.14879119G>T	GRCh38
NC_000011.9:g.14900665G>T , CM000673.1:g.14900665G>T	GRCh37
NC_000011.8:g.14857241G>T	NCBI36
NG_007936.1:g.18087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334636.10:c.1325C>A MANE Select	ENSP00000334592.5:p.Ser442Tyr
ENST00000334636.9:c.1325C>A	ENSP00000334592.5:p.Ser442Tyr
ENST00000525015.1:c.155C>A
ENST00000530609.5:c.*921C>A	ENSP00000466060.1:n.*921C>A
ENST00000532378.5:c.626C>A	ENSP00000435484.1:p.Ser209Tyr
ENST00000532805.1:c.*433C>A	ENSP00000465097.1:n.*433C>A
ENST00000534686.5:c.*685C>A	ENSP00000432087.2:n.*685C>A
NM_024514.4:c.1325C>A	NP_078790.2:p.Ser442Tyr
XM_005252788.1:c.1181C>A	XP_005252845.1:p.Ser394Tyr
XM_005252789.2:c.1163C>A	XP_005252846.1:p.Ser388Tyr
XM_005252791.3:c.980C>A	XP_005252848.1:p.Ser327Tyr
XM_006718142.2:c.1280C>A	XP_006718205.1:p.Ser427Tyr
XM_011519894.1:c.980C>A	XP_011518196.1:p.Ser327Tyr
XM_011519895.1:c.980C>A	XP_011518197.1:p.Ser327Tyr
XM_011519896.1:c.980C>A	XP_011518198.1:p.Ser327Tyr
XM_011519897.1:c.980C>A	XP_011518199.1:p.Ser327Tyr
XM_011519898.1:c.980C>A	XP_011518200.1:p.Ser327Tyr
XR_242777.2:n.1142C>A
XM_005252788.2:c.1181C>A	XP_005252845.1:p.Ser394Tyr
XM_005252789.3:c.1163C>A	XP_005252846.1:p.Ser388Tyr
XM_011519895.2:c.980C>A	XP_011518197.1:p.Ser327Tyr
XM_011519898.3:c.980C>A	XP_011518200.1:p.Ser327Tyr
XM_017017190.2:c.1160C>A	XP_016872679.1:p.Ser387Tyr
XM_017017191.2:c.980C>A	XP_016872680.1:p.Ser327Tyr
XM_017017192.2:c.980C>A	XP_016872681.1:p.Ser327Tyr
XM_017017193.2:c.980C>A	XP_016872682.1:p.Ser327Tyr
XM_017017194.2:c.980C>A	XP_016872683.1:p.Ser327Tyr
XM_024448345.1:c.1160C>A	XP_024304113.1:p.Ser387Tyr
XM_024448346.1:c.980C>A	XP_024304114.1:p.Ser327Tyr
XM_024448347.1:c.980C>A	XP_024304115.1:p.Ser327Tyr
XM_024448348.1:c.980C>A	XP_024304116.1:p.Ser327Tyr
XR_002957123.1:n.1105C>A
XR_002957124.1:n.1371C>A
XR_242777.3:n.1142C>A
NM_001377214.1:c.980C>A	NP_001364143.1:p.Ser327Tyr
NM_001377215.1:c.980C>A	NP_001364144.1:p.Ser327Tyr
NM_001377216.1:c.980C>A	NP_001364145.1:p.Ser327Tyr
NM_001377217.1:c.1163C>A	NP_001364146.1:p.Ser388Tyr
NM_001377227.1:c.980C>A	NP_001364156.1:p.Ser327Tyr
NM_024514.5:c.1325C>A MANE Select	NP_078790.2:p.Ser442Tyr
NM_001400558.1:c.980C>A	NP_001387487.1:p.Ser327Tyr
NM_001400559.1:c.980C>A	NP_001387488.1:p.Ser327Tyr
NM_001400560.1:c.980C>A	NP_001387489.1:p.Ser327Tyr
NM_001400561.1:c.980C>A	NP_001387490.1:p.Ser327Tyr
NM_001400562.1:c.626C>A	NP_001387491.1:p.Ser209Tyr
NM_001400563.1:c.626C>A	NP_001387492.1:p.Ser209Tyr
NM_001400564.1:c.626C>A	NP_001387493.1:p.Ser209Tyr
NM_001400565.1:c.626C>A	NP_001387494.1:p.Ser209Tyr
NM_001400566.1:c.347C>A	NP_001387495.1:p.Ser116Tyr
NM_001400567.1:c.1181C>A	NP_001387496.1:p.Ser394Tyr
NM_001400568.1:c.1280C>A	NP_001387497.1:p.Ser427Tyr
NR_174512.1:n.1192C>A
NR_174513.1:n.1041C>A
NR_174514.1:n.1416C>A
NR_174515.1:n.1825C>A
NR_174516.1:n.1003C>A
NR_174517.1:n.539C>A
NR_174518.1:n.1636C>A
NR_174519.1:n.1383C>A
NR_174520.1:n.1174C>A
NR_174521.1:n.1674C>A
NR_174522.1:n.1172C>A
NR_174523.1:n.1583C>A