Canonical Allele Identifier: CA6361899

Gene: PRDM10

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.129918648C>T , CM000673.2:g.129918648C>T	GRCh38
NC_000011.9:g.129788543C>T , CM000673.1:g.129788543C>T	GRCh37
NC_000011.8:g.129293753C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_199437.2:c.2105G>A MANE Select	NP_955469.1:p.Arg702His
ENST00000360871.8:c.2105G>A MANE Select	ENSP00000354118.3:p.Arg702His
NM_001367890.1:c.1757G>A	NP_001354819.1:p.Arg586His
NM_001367891.1:c.2045G>A	NP_001354820.1:p.Arg682His
NM_001367892.1:c.2051G>A	NP_001354821.1:p.Arg684His
NM_001367893.1:c.2117G>A	NP_001354822.1:p.Arg706His
NM_001367894.1:c.1757G>A	NP_001354823.1:p.Arg586His
NM_001367895.1:c.1256G>A	NP_001354824.1:p.Arg419His
NM_001367896.1:c.1256G>A	NP_001354825.1:p.Arg419His
NM_001367897.1:c.1268G>A	NP_001354826.1:p.Arg423His
NM_001367898.1:c.1847G>A	NP_001354827.1:p.Arg616His
NM_001367899.1:c.1859G>A	NP_001354828.1:p.Arg620His
NM_020228.2:c.2117G>A	NP_064613.2:p.Arg706His
NM_020228.3:c.2117G>A	NP_064613.2:p.Arg706His
NM_199437.1:c.2105G>A	NP_955469.1:p.Arg702His
NM_199438.1:c.1859G>A	NP_955470.1:p.Arg620His
NM_199438.2:c.1859G>A	NP_955470.1:p.Arg620His
NM_199439.1:c.1847G>A	NP_955471.1:p.Arg616His
NM_199439.2:c.1847G>A	NP_955471.1:p.Arg616His
ENST00000304538.10:c.1847G>A	ENSP00000302669.6:p.Arg616His
ENST00000358825.9:c.2117G>A	ENSP00000351686.5:p.Arg706His
ENST00000360871.7:c.2105G>A	ENSP00000354118.3:p.Arg702His
ENST00000423662.6:c.1859G>A	ENSP00000398431.2:p.Arg620His
ENST00000526082.5:c.1859G>A	ENSP00000432237.1:p.Arg620His
ENST00000528746.5:c.2027G>A	ENSP00000431262.1:p.Arg676His
ENST00000533431.1:c.1256G>A	ENSP00000435940.1:p.Arg419His
XM_011542912.1:c.2105G>A	XP_011541214.1:p.Arg702His
XM_011542912.2:c.2105G>A	XP_011541214.1:p.Arg702His
XM_011542913.1:c.2105G>A	XP_011541215.1:p.Arg702His
XM_011542914.1:c.1847G>A	XP_011541216.1:p.Arg616His
XM_011542915.1:c.1847G>A	XP_011541217.1:p.Arg616His
XM_011542916.1:c.1847G>A	XP_011541218.1:p.Arg616His
XM_017018023.1:c.1847G>A	XP_016873512.1:p.Arg616His