Canonical Allele Identifier: CA379745721

Gene: CYP2R1

Linked Data

• gnomAD v4: 11-14879395-G-T
• MyVariant Identifiers: chr11:g.14900941G>T (hg19) ; chr11:g.14879395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879395G>T , CM000673.2:g.14879395G>T	GRCh38
NC_000011.9:g.14900941G>T , CM000673.1:g.14900941G>T	GRCh37
NC_000011.8:g.14857517G>T	NCBI36
NG_007936.1:g.17811C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000334636.10:c.1049C>A MANE Select	ENSP00000334592.5:p.Pro350His
ENST00000334636.9:c.1049C>A	ENSP00000334592.5:p.Pro350His
ENST00000525015.1:c.67-188C>A
ENST00000530609.5:c.*645C>A	ENSP00000466060.1:n.*645C>A
ENST00000532378.5:c.350C>A	ENSP00000435484.1:p.Pro117His
ENST00000532805.1:c.*353-196C>A	ENSP00000465097.1:n.*353-196C>A
ENST00000534686.5:c.*597-188C>A	ENSP00000432087.2:n.*597-188C>A
NM_024514.4:c.1049C>A	NP_078790.2:p.Pro350His
XM_005252788.1:c.905C>A	XP_005252845.1:p.Pro302His
XM_005252789.2:c.887C>A	XP_005252846.1:p.Pro296His
XM_005252791.3:c.704C>A	XP_005252848.1:p.Pro235His
XM_006718142.2:c.1004C>A	XP_006718205.1:p.Pro335His
XM_011519894.1:c.704C>A	XP_011518196.1:p.Pro235His
XM_011519895.1:c.704C>A	XP_011518197.1:p.Pro235His
XM_011519896.1:c.704C>A	XP_011518198.1:p.Pro235His
XM_011519897.1:c.704C>A	XP_011518199.1:p.Pro235His
XM_011519898.1:c.704C>A	XP_011518200.1:p.Pro235His
XR_242777.2:n.1054-188C>A
XM_005252788.2:c.905C>A	XP_005252845.1:p.Pro302His
XM_005252789.3:c.887C>A	XP_005252846.1:p.Pro296His
XM_011519895.2:c.704C>A	XP_011518197.1:p.Pro235His
XM_011519898.3:c.704C>A	XP_011518200.1:p.Pro235His
XM_017017190.2:c.884C>A	XP_016872679.1:p.Pro295His
XM_017017191.2:c.704C>A	XP_016872680.1:p.Pro235His
XM_017017192.2:c.704C>A	XP_016872681.1:p.Pro235His
XM_017017193.2:c.704C>A	XP_016872682.1:p.Pro235His
XM_017017194.2:c.704C>A	XP_016872683.1:p.Pro235His
XM_024448345.1:c.884C>A	XP_024304113.1:p.Pro295His
XM_024448346.1:c.704C>A	XP_024304114.1:p.Pro235His
XM_024448347.1:c.704C>A	XP_024304115.1:p.Pro235His
XM_024448348.1:c.704C>A	XP_024304116.1:p.Pro235His
XR_002957123.1:n.1017-188C>A
XR_002957124.1:n.1283-188C>A
XR_242777.3:n.1054-188C>A
NM_001377214.1:c.704C>A	NP_001364143.1:p.Pro235His
NM_001377215.1:c.704C>A	NP_001364144.1:p.Pro235His
NM_001377216.1:c.704C>A	NP_001364145.1:p.Pro235His
NM_001377217.1:c.887C>A	NP_001364146.1:p.Pro296His
NM_001377227.1:c.704C>A	NP_001364156.1:p.Pro235His
NM_024514.5:c.1049C>A MANE Select	NP_078790.2:p.Pro350His
NM_001400558.1:c.704C>A	NP_001387487.1:p.Pro235His
NM_001400559.1:c.704C>A	NP_001387488.1:p.Pro235His
NM_001400560.1:c.704C>A	NP_001387489.1:p.Pro235His
NM_001400561.1:c.704C>A	NP_001387490.1:p.Pro235His
NM_001400562.1:c.350C>A	NP_001387491.1:p.Pro117His
NM_001400563.1:c.350C>A	NP_001387492.1:p.Pro117His
NM_001400564.1:c.350C>A	NP_001387493.1:p.Pro117His
NM_001400565.1:c.350C>A	NP_001387494.1:p.Pro117His
NM_001400566.1:c.71C>A	NP_001387495.1:p.Pro24His
NM_001400567.1:c.905C>A	NP_001387496.1:p.Pro302His
NM_001400568.1:c.1004C>A	NP_001387497.1:p.Pro335His
NR_174512.1:n.1104-188C>A
NR_174513.1:n.953-188C>A
NR_174514.1:n.1328-188C>A
NR_174515.1:n.1737-188C>A
NR_174516.1:n.915-188C>A
NR_174517.1:n.451-188C>A
NR_174518.1:n.1548-188C>A
NR_174519.1:n.1295-188C>A
NR_174520.1:n.1086-188C>A
NR_174521.1:n.1586-188C>A
NR_174522.1:n.1084-188C>A
NR_174523.1:n.1495-188C>A