Canonical Allele Identifier: CA10620010

Gene: PRDM5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.120781201C>G , CM000666.2:g.120781201C>G	GRCh38
NC_000004.11:g.121702356C>G , CM000666.1:g.121702356C>G	GRCh37
NC_000004.10:g.121921806C>G	NCBI36
NG_031862.2:g.146658G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_018699.4:c.1385G>C MANE Select	NP_061169.2:p.Arg462Thr
ENST00000264808.8:c.1385G>C MANE Select	ENSP00000264808.3:p.Arg462Thr
NM_001300823.1:c.1292G>C	NP_001287752.1:p.Arg431Thr
NM_001300823.2:c.1292G>C	NP_001287752.1:p.Arg431Thr
NM_001300824.1:c.1292G>C	NP_001287753.1:p.Arg431Thr
NM_001300824.2:c.1292G>C	NP_001287753.1:p.Arg431Thr
NM_001379104.1:c.1418G>C	NP_001366033.1:p.Arg473Thr
NM_001379106.1:c.1292G>C	NP_001366035.1:p.Arg431Thr
NM_018699.3:c.1385G>C	NP_061169.2:p.Arg462Thr
ENST00000264808.7:c.1385G>C	ENSP00000264808.3:p.Arg462Thr
ENST00000428209.6:c.1292G>C	ENSP00000404832.2:p.Arg431Thr
ENST00000505484.5:n.1715G>C
ENST00000515109.5:c.1292G>C	ENSP00000422309.1:p.Arg431Thr
XM_011531562.1:c.1418G>C	XP_011529864.1:p.Arg473Thr
XM_011531562.2:c.1418G>C	XP_011529864.1:p.Arg473Thr
XM_011531563.1:c.1325G>C	XP_011529865.1:p.Arg442Thr
XM_011531563.2:c.1325G>C	XP_011529865.1:p.Arg442Thr
XM_011531564.1:c.1418G>C	XP_011529866.1:p.Arg473Thr
XM_011531564.2:c.1418G>C	XP_011529866.1:p.Arg473Thr
XM_011531565.1:c.1418G>C	XP_011529867.1:p.Arg473Thr
XM_011531565.2:c.1418G>C	XP_011529867.1:p.Arg473Thr
XM_011531566.1:c.1418G>C	XP_011529868.1:p.Arg473Thr
XM_011531566.3:c.1418G>C	XP_011529868.1:p.Arg473Thr
XM_011531567.1:c.1418G>C	XP_011529869.1:p.Arg473Thr
XM_011531567.2:c.1418G>C	XP_011529869.1:p.Arg473Thr
XM_011531568.1:c.1418G>C	XP_011529870.1:p.Arg473Thr
XM_011531568.2:c.1418G>C	XP_011529870.1:p.Arg473Thr
XM_011531569.1:c.1418G>C	XP_011529871.1:p.Arg473Thr
XM_011531569.3:c.1418G>C	XP_011529871.1:p.Arg473Thr
XM_011531570.1:c.704G>C	XP_011529872.1:p.Arg235Thr
XM_011531570.3:c.704G>C	XP_011529872.1:p.Arg235Thr
XM_017007668.2:c.1340G>C	XP_016863157.1:p.Arg447Thr
XM_017007669.1:c.1385G>C	XP_016863158.1:p.Arg462Thr
XM_017007670.1:c.1385G>C	XP_016863159.1:p.Arg462Thr
XM_017007671.1:c.443G>C	XP_016863160.1:p.Arg148Thr
XM_024453879.1:c.671G>C	XP_024309647.1:p.Arg224Thr
XR_938677.1:n.1659G>C
XR_938677.3:n.1659G>C
XR_938678.1:n.1659G>C
XR_938679.1:n.1659G>C
XR_938680.1:n.1659G>C
XR_938680.2:n.1659G>C