Canonical Allele Identifier: CA1953974326

Gene: CYP2R1

Linked Data

• dbSNP Id: rs1412954083
• gnomAD v4: 11-14879571-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14879577del , CM000673.2:g.14879577del	GRCh38
NC_000011.9:g.14901123del , CM000673.1:g.14901123del	GRCh37
NC_000011.8:g.14857699del	NCBI36
NG_007936.1:g.17634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334636.10:c.1001-129del MANE Select	ENSP00000334592.5:n.1001-129del
ENST00000334636.9:c.1001-129del	ENSP00000334592.5:n.1001-129del
ENST00000525015.1:c.67-365del
ENST00000530609.5:c.*597-129del	ENSP00000466060.1:n.*597-129del
ENST00000532378.5:c.302-129del	ENSP00000435484.1:n.302-129del
ENST00000532805.1:c.*353-373del	ENSP00000465097.1:n.*353-373del
ENST00000534686.5:c.*597-365del	ENSP00000432087.2:n.*597-365del
NM_024514.4:c.1001-129del	NP_078790.2:n.1001-129del
XM_005252788.1:c.857-129del	XP_005252845.1:n.857-129del
XM_005252789.2:c.839-129del	XP_005252846.1:n.839-129del
XM_005252791.3:c.656-129del	XP_005252848.1:n.656-129del
XM_006718142.2:c.956-129del	XP_006718205.1:n.956-129del
XM_011519894.1:c.656-129del	XP_011518196.1:n.656-129del
XM_011519895.1:c.656-129del	XP_011518197.1:n.656-129del
XM_011519896.1:c.656-129del	XP_011518198.1:n.656-129del
XM_011519897.1:c.656-129del	XP_011518199.1:n.656-129del
XM_011519898.1:c.656-129del	XP_011518200.1:n.656-129del
XR_242777.2:n.1054-365del
XM_005252788.2:c.857-129del	XP_005252845.1:n.857-129del
XM_005252789.3:c.839-129del	XP_005252846.1:n.839-129del
XM_011519895.2:c.656-129del	XP_011518197.1:n.656-129del
XM_011519898.3:c.656-129del	XP_011518200.1:n.656-129del
XM_017017190.2:c.836-129del	XP_016872679.1:n.836-129del
XM_017017191.2:c.656-129del	XP_016872680.1:n.656-129del
XM_017017192.2:c.656-129del	XP_016872681.1:n.656-129del
XM_017017193.2:c.656-129del	XP_016872682.1:n.656-129del
XM_017017194.2:c.656-129del	XP_016872683.1:n.656-129del
XM_024448345.1:c.836-129del	XP_024304113.1:n.836-129del
XM_024448346.1:c.656-129del	XP_024304114.1:n.656-129del
XM_024448347.1:c.656-129del	XP_024304115.1:n.656-129del
XM_024448348.1:c.656-129del	XP_024304116.1:n.656-129del
XR_002957123.1:n.1017-365del
XR_002957124.1:n.1283-365del
XR_242777.3:n.1054-365del
NM_001377214.1:c.656-129del	NP_001364143.1:n.656-129del
NM_001377215.1:c.656-129del	NP_001364144.1:n.656-129del
NM_001377216.1:c.656-129del	NP_001364145.1:n.656-129del
NM_001377217.1:c.839-129del	NP_001364146.1:n.839-129del
NM_001377227.1:c.656-129del	NP_001364156.1:n.656-129del
NM_024514.5:c.1001-129del MANE Select	NP_078790.2:n.1001-129del
NM_001400558.1:c.656-129del	NP_001387487.1:n.656-129del
NM_001400559.1:c.656-129del	NP_001387488.1:n.656-129del
NM_001400560.1:c.656-129del	NP_001387489.1:n.656-129del
NM_001400561.1:c.656-129del	NP_001387490.1:n.656-129del
NM_001400562.1:c.302-129del	NP_001387491.1:n.302-129del
NM_001400563.1:c.302-129del	NP_001387492.1:n.302-129del
NM_001400564.1:c.302-129del	NP_001387493.1:n.302-129del
NM_001400565.1:c.302-129del	NP_001387494.1:n.302-129del
NM_001400566.1:c.23-129del	NP_001387495.1:n.23-129del
NM_001400567.1:c.857-129del	NP_001387496.1:n.857-129del
NM_001400568.1:c.956-129del	NP_001387497.1:n.956-129del
NR_174512.1:n.1104-365del
NR_174513.1:n.953-365del
NR_174514.1:n.1328-365del
NR_174515.1:n.1737-365del
NR_174516.1:n.915-365del
NR_174517.1:n.451-365del
NR_174518.1:n.1548-365del
NR_174519.1:n.1295-365del
NR_174520.1:n.1086-365del
NR_174521.1:n.1586-365del
NR_174522.1:n.1084-365del
NR_174523.1:n.1495-365del