Canonical Allele Identifier: CA379744639

Gene: CYP2R1

Linked Data

• MyVariant Identifiers: chr11:g.14900658A>G (hg19) ; chr11:g.14879112A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879112A>G , CM000673.2:g.14879112A>G	GRCh38
NC_000011.9:g.14900658A>G , CM000673.1:g.14900658A>G	GRCh37
NC_000011.8:g.14857234A>G	NCBI36
NG_007936.1:g.18094T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334636.10:c.1330+2T>C MANE Select	ENSP00000334592.5:n.1330+2T>C
ENST00000334636.9:c.1330+2T>C	ENSP00000334592.5:n.1330+2T>C
ENST00000525015.1:c.160+2T>C
ENST00000530609.5:c.*926+2T>C	ENSP00000466060.1:n.*926+2T>C
ENST00000532378.5:c.631+2T>C	ENSP00000435484.1:n.631+2T>C
ENST00000532805.1:c.*438+2T>C	ENSP00000465097.1:n.*438+2T>C
ENST00000534686.5:c.*690+2T>C	ENSP00000432087.2:n.*690+2T>C
NM_024514.4:c.1330+2T>C	NP_078790.2:n.1330+2T>C
XM_005252788.1:c.1186+2T>C	XP_005252845.1:n.1186+2T>C
XM_005252789.2:c.1168+2T>C	XP_005252846.1:n.1168+2T>C
XM_005252791.3:c.985+2T>C	XP_005252848.1:n.985+2T>C
XM_006718142.2:c.1285+2T>C	XP_006718205.1:n.1285+2T>C
XM_011519894.1:c.985+2T>C	XP_011518196.1:n.985+2T>C
XM_011519895.1:c.985+2T>C	XP_011518197.1:n.985+2T>C
XM_011519896.1:c.985+2T>C	XP_011518198.1:n.985+2T>C
XM_011519897.1:c.985+2T>C	XP_011518199.1:n.985+2T>C
XM_011519898.1:c.985+2T>C	XP_011518200.1:n.985+2T>C
XR_242777.2:n.1147+2T>C
XM_005252788.2:c.1186+2T>C	XP_005252845.1:n.1186+2T>C
XM_005252789.3:c.1168+2T>C	XP_005252846.1:n.1168+2T>C
XM_011519895.2:c.985+2T>C	XP_011518197.1:n.985+2T>C
XM_011519898.3:c.985+2T>C	XP_011518200.1:n.985+2T>C
XM_017017190.2:c.1165+2T>C	XP_016872679.1:n.1165+2T>C
XM_017017191.2:c.985+2T>C	XP_016872680.1:n.985+2T>C
XM_017017192.2:c.985+2T>C	XP_016872681.1:n.985+2T>C
XM_017017193.2:c.985+2T>C	XP_016872682.1:n.985+2T>C
XM_017017194.2:c.985+2T>C	XP_016872683.1:n.985+2T>C
XM_024448345.1:c.1165+2T>C	XP_024304113.1:n.1165+2T>C
XM_024448346.1:c.985+2T>C	XP_024304114.1:n.985+2T>C
XM_024448347.1:c.985+2T>C	XP_024304115.1:n.985+2T>C
XM_024448348.1:c.985+2T>C	XP_024304116.1:n.985+2T>C
XR_002957123.1:n.1110+2T>C
XR_002957124.1:n.1376+2T>C
XR_242777.3:n.1147+2T>C
NM_001377214.1:c.985+2T>C	NP_001364143.1:n.985+2T>C
NM_001377215.1:c.985+2T>C	NP_001364144.1:n.985+2T>C
NM_001377216.1:c.985+2T>C	NP_001364145.1:n.985+2T>C
NM_001377217.1:c.1168+2T>C	NP_001364146.1:n.1168+2T>C
NM_001377227.1:c.985+2T>C	NP_001364156.1:n.985+2T>C
NM_024514.5:c.1330+2T>C MANE Select	NP_078790.2:n.1330+2T>C
NM_001400558.1:c.985+2T>C	NP_001387487.1:n.985+2T>C
NM_001400559.1:c.985+2T>C	NP_001387488.1:n.985+2T>C
NM_001400560.1:c.985+2T>C	NP_001387489.1:n.985+2T>C
NM_001400561.1:c.985+2T>C	NP_001387490.1:n.985+2T>C
NM_001400562.1:c.631+2T>C	NP_001387491.1:n.631+2T>C
NM_001400563.1:c.631+2T>C	NP_001387492.1:n.631+2T>C
NM_001400564.1:c.631+2T>C	NP_001387493.1:n.631+2T>C
NM_001400565.1:c.631+2T>C	NP_001387494.1:n.631+2T>C
NM_001400566.1:c.352+2T>C	NP_001387495.1:n.352+2T>C
NM_001400567.1:c.1186+2T>C	NP_001387496.1:n.1186+2T>C
NM_001400568.1:c.1285+2T>C	NP_001387497.1:n.1285+2T>C
NR_174512.1:n.1197+2T>C
NR_174513.1:n.1046+2T>C
NR_174514.1:n.1421+2T>C
NR_174515.1:n.1830+2T>C
NR_174516.1:n.1008+2T>C
NR_174517.1:n.544+2T>C
NR_174518.1:n.1641+2T>C
NR_174519.1:n.1388+2T>C
NR_174520.1:n.1179+2T>C
NR_174521.1:n.1679+2T>C
NR_174522.1:n.1177+2T>C
NR_174523.1:n.1588+2T>C