Canonical Allele Identifier: CA358207840

Gene: PRDM5

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.120816917G>A , CM000666.2:g.120816917G>A	GRCh38
NC_000004.11:g.121738072G>A , CM000666.1:g.121738072G>A	GRCh37
NC_000004.10:g.121957522G>A	NCBI36
NG_031862.2:g.110942C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_018699.4:c.658C>T MANE Select	NP_061169.2:p.Gln220Ter
ENST00000264808.8:c.658C>T MANE Select	ENSP00000264808.3:p.Gln220Ter
NM_001300823.1:c.651-343C>T	NP_001287752.1:n.651-343C>T
NM_001300823.2:c.651-343C>T	NP_001287752.1:n.651-343C>T
NM_001300824.1:c.651-343C>T	NP_001287753.1:n.651-343C>T
NM_001300824.2:c.651-343C>T	NP_001287753.1:n.651-343C>T
NM_001379104.1:c.658C>T	NP_001366033.1:p.Gln220Ter
NM_001379106.1:c.651-343C>T	NP_001366035.1:n.651-343C>T
NM_018699.3:c.658C>T	NP_061169.2:p.Gln220Ter
ENST00000264808.7:c.658C>T	ENSP00000264808.3:p.Gln220Ter
ENST00000428209.6:c.651-343C>T	ENSP00000404832.2:n.651-343C>T
ENST00000502409.1:c.189C>T
ENST00000505484.5:n.731C>T
ENST00000512845.5:n.738-343C>T
ENST00000515109.5:c.651-343C>T	ENSP00000422309.1:n.651-343C>T
XM_005262708.2:c.658C>T	XP_005262765.1:p.Gln220Ter
XM_005262708.3:c.658C>T	XP_005262765.1:p.Gln220Ter
XM_011531562.1:c.658C>T	XP_011529864.1:p.Gln220Ter
XM_011531562.2:c.658C>T	XP_011529864.1:p.Gln220Ter
XM_011531563.1:c.651-343C>T	XP_011529865.1:n.651-343C>T
XM_011531563.2:c.651-343C>T	XP_011529865.1:n.651-343C>T
XM_011531564.1:c.658C>T	XP_011529866.1:p.Gln220Ter
XM_011531564.2:c.658C>T	XP_011529866.1:p.Gln220Ter
XM_011531565.1:c.658C>T	XP_011529867.1:p.Gln220Ter
XM_011531565.2:c.658C>T	XP_011529867.1:p.Gln220Ter
XM_011531566.1:c.658C>T	XP_011529868.1:p.Gln220Ter
XM_011531566.3:c.658C>T	XP_011529868.1:p.Gln220Ter
XM_011531567.1:c.658C>T	XP_011529869.1:p.Gln220Ter
XM_011531567.2:c.658C>T	XP_011529869.1:p.Gln220Ter
XM_011531568.1:c.658C>T	XP_011529870.1:p.Gln220Ter
XM_011531568.2:c.658C>T	XP_011529870.1:p.Gln220Ter
XM_011531569.1:c.658C>T	XP_011529871.1:p.Gln220Ter
XM_011531569.3:c.658C>T	XP_011529871.1:p.Gln220Ter
XM_011531570.1:c.151+1436C>T	XP_011529872.1:n.151+1436C>T
XM_011531570.3:c.151+1436C>T	XP_011529872.1:n.151+1436C>T
XM_017007668.2:c.580C>T	XP_016863157.1:p.Gln194Ter
XM_017007669.1:c.658C>T	XP_016863158.1:p.Gln220Ter
XM_017007670.1:c.658C>T	XP_016863159.1:p.Gln220Ter
XM_024453879.1:c.151+1436C>T	XP_024309647.1:n.151+1436C>T
XR_938677.1:n.899C>T
XR_938677.3:n.899C>T
XR_938678.1:n.899C>T
XR_938679.1:n.899C>T
XR_938680.1:n.899C>T
XR_938680.2:n.899C>T